Processes of preparing a JAK1 inhibitor and new forms thereto

ABSTRACT

This invention relates to processes for preparing a JAK1 inhibitor having Formula Ia: 
                         
as well as new forms of the inhibitor.

This application claims the benefit of priority of Ser. No. 61/986,738, filed Apr. 30, 2014, and Ser. No. 61/986,789, filed Apr. 30, 2014, each of which is incorporated herein by reference in its entirety.

TECHNICAL FIELD

This invention relates to processes for preparing a JAK1 inhibitor, as well as new forms of the inhibitor.

BACKGROUND

Protein kinases (PKs) regulate diverse biological processes including cell growth, survival, differentiation, organ formation, morphogenesis, neovascularization, tissue repair, and regeneration, among others. Protein kinases also play specialized roles in a host of human diseases including cancer. Cytokines, low-molecular weight polypeptides or glycoproteins, regulate many pathways involved in the host inflammatory response to sepsis. Cytokines influence cell differentiation, proliferation and activation, and can modulate both pro-inflammatory and anti-inflammatory responses to allow the host to react appropriately to pathogens. Signaling of a wide range of cytokines involves the Janus kinase family (JAKs) of protein tyrosine kinases and Signal Transducers and Activators of Transcription (STATs). There are four known mammalian JAKs: JAK1 (Janus kinase-1), JAK2, JAK3 (also known as Janus kinase, leukocyte; JAKL; and L-JAK), and TYK2 (protein-tyrosine kinase 2).

Cytokine-stimulated immune and inflammatory responses contribute to pathogenesis of diseases: pathologies such as severe combined immunodeficiency (SCID) arise from suppression of the immune system, while a hyperactive or inappropriate immune/inflammatory response contributes to the pathology of autoimmune diseases (e.g., asthma, systemic lupus erythematosus, thyroiditis, myocarditis), and illnesses such as scleroderma and osteoarthritis (Ortmann, R. A., T. Cheng, et al. (2000) Arthritis Res 2(1): 16-32).

Deficiencies in expression of JAKs are associated with many disease states. For example, Jak1−/− mice are runted at birth, fail to nurse, and die perinatally (Rodig, S. J., M. A. Meraz, et al. (1998) Cell 93(3): 373-83). Jak2−/− mouse embryos are anemic and die around day 12.5 postcoitum due to the absence of definitive erythropoiesis.

The JAK/STAT pathway, and in particular all four JAKs, are believed to play a role in the pathogenesis of asthmatic response, chronic obstructive pulmonary disease, bronchitis, and other related inflammatory diseases of the lower respiratory tract. Multiple cytokines that signal through JAKs have been linked to inflammatory diseases/conditions of the upper respiratory tract, such as those affecting the nose and sinuses (e.g., rhinitis and sinusitis) whether classically allergic reactions or not. The JAK/STAT pathway has also been implicated in inflammatory diseases/conditions of the eye and chronic allergic responses.

Activation of JAK/STAT in cancers may occur by cytokine stimulation (e.g. IL-6 or GM-CSF) or by a reduction in the endogenous suppressors of JAK signaling such as SOCS (suppressor or cytokine signaling) or PIAS (protein inhibitor of activated STAT) (Boudny, V., and Kovarik, J., Neoplasm. 49:349-355, 2002). Activation of STAT signaling, as well as other pathways downstream of JAKs (e.g., Akt), has been correlated with poor prognosis in many cancer types (Bowman, T., et al. Oncogene 19:2474-2488, 2000). Elevated levels of circulating cytokines that signal through JAK/STAT play a causal role in cachexia and/or chronic fatigue. As such, JAK inhibition may be beneficial to cancer patients for reasons that extend beyond potential anti-tumor activity.

JAK2 tyrosine kinase can be beneficial for patients with myeloproliferative disorders, e.g., polycythemia vera (PV), essential thrombocythemia (ET), myeloid metaplasia with myelofibrosis (MMM) (Levin, et al., Cancer Cell, vol. 7, 2005: 387-397). Inhibition of the JAK2V617F kinase decreases proliferation of hematopoietic cells, suggesting JAK2 as a potential target for pharmacologic inhibition in patients with PV, ET, and MMM.

Inhibition of the JAKs may benefit patients suffering from skin immune disorders such as psoriasis, and skin sensitization. The maintenance of psoriasis is believed to depend on a number of inflammatory cytokines in addition to various chemokines and growth factors (JCI, 113:1664-1675), many of which signal through JAKs (Adv Pharmacol. 2000; 47:113-74).

Thus, new or improved agents which inhibit kinases such as JAKs are continually needed for developing new and more effective pharmaceuticals that are aimed at augmentation or suppression of the immune and inflammatory pathways (such as immunosuppressive agents for organ transplants), as well as agents for the prevention and treatment of autoimmune diseases, diseases involving a hyperactive inflammatory response (e.g., eczema), allergies, cancer (e.g., prostate, leukemia, multiple myeloma), and some immune reactions (e.g., skin rash or contact dermatitis or diarrhea) caused by other therapeutics. The compounds of the invention, as well as its compositions and methods described herein are directed toward these needs and other ends.

SUMMARY

The present invention provides process of preparing a compound of Formula Ia:

comprising reacting a compound of Formula Ib:

with a strong base in the presence of a first solvent component.

The present application provides an anhydrous form of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile.

The present application also provides a monohydrate form of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile.

The present application further provides various intermediates useful in the synthesis of the compound of Formula Ia.

DESCRIPTION OF DRAWINGS

FIG. 1 shows a DSC thermogram characteristic of the compound of Example 9.

FIG. 2 shows a TGA thermogram characteristic of the compound of Example 9.

FIG. 3 shows an XRPD pattern characteristic of the compound of Example 9.

FIG. 4 shows a DSC thermogram characteristic of the compound of Example 10.

FIG. 5 shows a TGA thermogram characteristic of the compound of Example 10.

FIG. 6 shows an XRPD pattern characteristic of the compound of Example 10.

FIG. 7 shows a Vapor Sorption/Desorption Isotherm (1^(st) cycle) characteristic of the compound of Example 9.

FIG. 8 shows a Vapor Sorption/Desorption Isotherm (4^(th) cycle) characteristic of the compound of Example 9.

FIG. 9 shows an XRPD pattern overlay of the compound of Example 9 before and after a Dynamic Vapor Sorption (DVS) study.

FIG. 10 shows an XRPD pattern characteristic of the compound of Example 9 after 5 days in a humidity chamber set at 75% relative humidity and 40° C.

FIG. 11 shows a TGA thermogram characteristic of the compound of Example 9 after 5 days in a humidity chamber set at 75% relative humidity and 40° C.

FIG. 12 shows a DSC thermogram of the compound of Example 9 after 5 days in a humidity chamber set at 75% relative humidity and 40° C.

FIG. 13 shows an XRPD pattern characteristic of the compound of Example 9 after 7 days in a humidity chamber set at 90% relative humidity and 30° C.

FIG. 14 shows a TGA thermogram of the compound of Example 9 after 7 days in a humidity chamber set at 90% relative humidity and 30° C.

FIG. 15 shows a DSC thermogram of the compound of Example 9 after 7 days in a humidity chamber set at 90% relative humidity and 30° C.

DETAILED DESCRIPTION

The present invention provides, inter alia, processes and intermediates for making 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, which is a compound Formula Ia:

as well as new forms of the compound of Formula Ia. The compound of Formula Ia includes anhydrous and hydrated forms of the compound. For example, the present application provides a new anhydrous form and a new monohydrate form of the compound of Formula Ia. The monohydrate form has Formula II:

The present application provides an anhydrous form of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile.

In some embodiments, the anhydrous form is substantially isolated. In some embodiments, the anhydrous form is crystalline.

In some embodiments, the anhydrous form is characterized by a differential scanning cal thermogram having an endothermic peak having an onset at about 185° C. In some embodiments, the anhydrous form is characterized by a differential scanning calorimetry (DSC) thermogram having an endothermic peak at about 190° C. In some embodiments, the anhydrous form has a DSC thermogram substantially as shown in FIG. 1.

In some embodiments, the anhydrous form is characterized by a thermogravimetric analysis (TGA) thermogram having a weight loss of about 1.25% up to 200° C. In some embodiments, the anhydrous form has a TGA thermogram substantially as shown in FIG. 2.

In some embodiments, the anhydrous form has at least one XRPD peak, in terms of 2-theta, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°. In some embodiments, the anhydrous form has at least two XRPD peaks, in terms of 2-theta, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°. In some embodiments, the anhydrous form has at least three XRPD peaks, in terms of 2-theta, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°. In some embodiments, the anhydrous form has at least four XRPD peaks, in terms of 2-theta, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°. In some embodiments, the anhydrous form has at least four XRPD peaks, in terms of 2-theta, selected from about 8.8°, about 16.3°, about 19.1°, about 24.0°, and about 26.4°.

In some embodiments, the anhydrous form has an XRPD pattern substantially as shown in FIG. 3. In some embodiments, the anhydrous form has a Vapor Sorption/Desorption Isotherm substantially as shown in FIG. 7. In some embodiments, the anhydrous form has a Vapor Sorption/Desorption Isotherm substantially as shown in FIG. 8.

The present application also provides a monohydrate form of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate, which is a compound of Formula II:

In some embodiments, the monohydrate form has a water content of about 5%. In some embodiments, the monohydrate form is substantially isolated. In some embodiments, the monohydrate form is crystalline.

In some embodiments, the monohydrate form is characterized by a DSC thermogram having an endothermic peak having an onset at about 69° C. In some embodiments, the monohydrate form is characterized by a DSC thermogram having an endothermic peak at about 106° C.

In some embodiments, the monohydrate form is characterized by a DSC thermogram having an endothermic peak having an onset at about 131° C. In some embodiments, the monohydrate form is characterized by a DSC thermogram having an endothermic peak at about 140° C. In some embodiments, the monohydrate form has a DSC thermogram substantially as shown in FIG. 4.

In some embodiments, the monohydrate form is characterized by a TGA thermogram having a weight loss of about 5% up to about 150° C. In some embodiments, the monohydrate form has a TGA thermogram substantially as shown in FIG. 5.

In some embodiments, the monohydrate form has at least one XRPD peak, in terms of 2-theta, selected from about 8.5°, about 8.7°, about 14.6°, about 15.1°, about 19.4°, about 25.1°, and about 26.5°. In some embodiments, the monohydrate form has at least two XRPD peaks, in terms of 2-theta, selected from about 8.5°, about 8.7°, about 14.6°, about 15.1°, about 19.4°, about 25.1°, and about 26.5°. In some embodiments, the monohydrate form has at least three XRPD peaks, in terms of 2-theta, selected from about 8.5°, about 8.7°, about 14.6°, about 15.1°, about 19.4°, about 25.1°, and about 26.5°. In some embodiments, the monohydrate form has at least four XRPD peaks, in terms of 2-theta, selected from about 8.5°, about 8.7°, about 14.6°, about 15.1°, about 19.4°, about 25.1°, and about 26.5°. In some embodiments, the monohydrate form has an XRPD pattern substantially as shown in FIG. 6.

An XRPD pattern of reflections (peaks) is typically considered a fingerprint of a particular crystalline form. It is well known that the relative intensities of the XRPD peaks can widely vary depending on, inter alia, the sample preparation technique, crystal size distribution, various filters used, the sample mounting procedure, and the particular instrument employed. In some instances, new peaks may be observed or existing peaks may disappear, depending on the type of the instrument or the settings. As used herein, the term “peak” refers to a reflection having a relative height/intensity of at least about 4% of the maximum peak height/intensity. Moreover, instrument variation and other factors can affect the 2-theta values. Thus, peak assignments, such as those reported herein, can vary by plus or minus about 0.2° (2-theta), and the term “substantially” and “about” as used in the context of XRPD herein is meant to encompass the above-mentioned variations.

In the same way, temperature readings in connection with DSC, TGA, or other thermal experiments can vary about ±3° C. depending on the instrument, particular settings, sample preparation, etc. Accordingly, a crystalline form reported herein having a DSC thermogram “substantially” as shown in any of the Figures or the term “about” is understood to accommodate such variation.

The present application further provides a process of forming the anhydrous form of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, comprising:

(i) adding n-heptane to a first mixture comprising a compound of Formula II:

and a first solvent component, wherein the first solvent component comprises ethyl acetate.

In some embodiments, the first solvent component further comprises methanol.

In some embodiments, the process further comprises before (i):

(ii) dissolving the compound of Formula II in methanol to form a second mixture comprising the compound of Formula Ia and a second solvent component comprising methanol;

(iii) polish filtering the second mixture; and

(iv) adding ethyl acetate to the second mixture to form the first mixture.

In some embodiments, the process further comprises heating the first mixture to a temperature from about 60° C. to about 75° C.

In some embodiments, the process further comprises removing at least a portion of the ethyl acetate and methanol to form the first mixture via distillation.

The present application further provides a process of preparing a compound of Formula Ia:

comprising reacting a compound of Formula Ib:

with a strong base in the presence of a first solvent component.

In some embodiments, the strong base is an alkoxide base.

In some embodiments, the strong base is an alkali metal C₁₋₆ alkoxide.

In some embodiments, the strong base is potassium tert-butoxide.

In some embodiments, the first solvent component comprises isopropyl alcohol.

In some embodiments, the first solvent component comprises isopropyl alcohol and tetrahydrofuran.

In some embodiments, the reacting of the composition with the strong base is conducted at a temperature of about room temperature.

In some embodiments, wherein about 0.05 to about 0.15 equivalents of strong base is used based on 1 equivalent of the compound of Formula Ib.

In some embodiments, the compound of Formula Ib is present in a composition comprising the compound of Formula Ib and the compound of Formula Ia prior to said reacting of said compound of Formula Ib with said strong base.

In some embodiments, the strong base that is reacted with a compound of Formula Ib is referred to as a first strong base.

In some embodiments, the compound of Formula Ia is prepared as a compound of Formula II:

In some embodiments, the composition comprising a compound of Formula Ia and a compound of Formula Ib is prepared by a process comprising reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb:

with a compound of Formula IV:

in the presence of a C₁₋₆ alkyloxonium reagent and a second solvent component.

In some embodiments, before reacting, the compound of Formula IV is reacted with said C₁₋₆ alkyloxonium reagent in the second solvent component.

In some embodiments, the reacting step is referred to as the reacting of a composition comprising a compound of Formula IIIa and a compound of Formula IIIb.

In some embodiments, the C₁₋₆ alkyloxonium reagent is triethyloxonium tetrafluoroborate.

In some embodiments, the second solvent component comprises ethanol.

In some embodiments, the second solvent component comprises tetrahydrofuran.

In some embodiments, the second solvent component comprises ethanol and tetrahydrofuran.

In some embodiments, the reacting of the composition of the compound of Formula IIIa and the compound of Formula IIIb with the compound of Formula IV is conducted at a temperature at reflux.

In some embodiments, about 2 to about 4 equivalents of the compound of Formula IV is used based on 1 equivalent of the combined amount of the compound of Formula IIIa and the compound of Formula IIIb.

In some embodiments, about 2 to about 4 equivalents of the alkyloxonium reagent is used based on 1 equivalent of the combined amount of the compound of Formula IIIa and the compound of Formula IIIb.

In some embodiments, the composition comprising a compound of Formula IIIa and a compound of Formula IIIb is prepared by a process comprising reacting a composition comprising a compound of Formula Va and a compound of Formula Vb:

with hydrogen gas in the presence of a hydrogenation catalyst and a third solvent component.

In some embodiments, the hydrogenation catalyst is palladium on carbon.

In some embodiments, the third solvent component comprises 2,2,2-trifluoroethanol.

In some embodiments, the reacting is run at a temperature from about 20° C. to about 35° C.

In some embodiments, the reacting step is referred to as the reacting of a composition comprising a compound of Formula Va and a compound of Formula Vb.

In some embodiments, about 5 to about 15 weight % of the hydrogenation catalyst is used based on total mass of the compound of Formula Va and the compound of Formula Vb.

In some embodiments, the composition comprising a compound of Formula Va and a compound of Formula Vb is prepared by a process comprising reacting a compound of Formula VI:

or a salt thereof, with a compound of Formula VII:

in the presence of an tertiary amine base and a fourth solvent component, wherein:

X is a halo group.

In some embodiments, the compound of Formula VI, or salt thereof, is a salt of Formula VIa:

In some embodiments, X is chloro.

In some embodiments, the tertiary amine base is N-ethyl-N-isopropylpropan-2-amine.

In some embodiments, the tertiary amine base that is present in the reaction of the compound of Formula VI is referred to as a first tertiary amine base.

In some embodiments, the fourth solvent component comprises N,N-dimethylformamide.

In some embodiments, the reacting is run at a temperature from about 65° C. to about 75° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula VI.

In some embodiments, the compound of Formula VI, or salt thereof, is a salt of Formula VIa:

the fourth solvent component comprises N,N-dimethylformamide;

the tertiary amine base is N-ethyl-N-isopropylpropan-2-amine; and

X is chloro.

The present application further provides a process of preparing a compound of Formula VI, comprising reacting a compound of Formula VIII:

under deprotection conditions to form the compound of Formula VI, or a salt thereof;

wherein P¹ is an amine protecting group.

In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the deprotection conditions involve reacting the compound of Formula VIII with a strong acid.

In some embodiments, the strong acid is HCl.

In some embodiments, the strong acid that is reacted with a compound of Formula VIII is referred to as a first strong acid.

In some embodiments, the reacting is run at a temperature from about 0° C. to about 40° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula VIII.

In some embodiments, the compound of Formula VIII is prepared by a process comprising reacting a compound of Formula IX:

in the presence of a strong base and a fifth solvent component, wherein

indicates a cis- or trans-bond; and P¹ is an amine protecting group. In some embodiments, the P¹ is t-butoxycarbonyl.

In some embodiments, the strong base is a C₁₋₆ alkoxide base.

In some embodiments, the alkoxide base is an alkali metal C₁₋₆ alkoxide.

In some embodiments, the alkoxide base is sodium methoxide.

In some embodiments, the strong base is present in a catalytic amount.

In some embodiments, the catalytic amount comprises about 0.010 to about 0.020 equivalents of the strong base based on 1 equivalent of the compound of Formula IX.

In some embodiments, the strong base that is present in the reaction of the compound of Formula IX is referred to as a second strong base.

In some embodiments, the fifth solvent component comprises tetrahydrofuran.

In some embodiments, the reacting is run at a temperature from about 0° C. to 5° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula IX.

In some embodiments, the compound of Formula IX is prepared by a process comprising reacting a compound of Formula X:

in the presence of a strong acid and a sixth solvent component, wherein

indicates a cis- or trans-bond; and P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the strong acid is p-toluenesulfonic acid.

In some embodiments, the strong acid is present in a catalytic amount.

In some embodiments, the catalytic amount comprises about 0.005 to about 0.015 equivalents of the strong acid based on 1 equivalent of the compound of Formula X.

In some embodiments, the strong acid that is present in the reaction of the compound of Formula X is referred to as a second strong acid.

In some embodiments, the sixth solvent component comprises methanol.

In some embodiments, the reacting of the compound of Formula X in the presence of the strong acid is run at a temperature of about room temperature.

In some embodiments, the compound of Formula X is prepared by a process comprising:

(i) reacting a compound of Formula XII:

with a Wittig reagent in the presence of a seventh solvent component, wherein said Wittig reagent is prepared by a process comprising reacting a compound of Formula XXI:

in the presence of a strong base, wherein R^(a) and R^(b) are each independently C₁₋₆ alkyl; and

P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, before (i), the compound of Formula XXI is reacted with the strong base in said second solvent component.

In some embodiments, R^(a) and R^(b) are each ethyl.

In some embodiments, the strong base is potassium tert-butoxide.

In some embodiments, the strong base that is present in the reaction of the compound of Formula XXI is referred to as a base.

In some embodiments, the seventh solvent component comprises tetrahydrofuran.

In some embodiments, the reacting is run at a temperature at about 0° C. to about 5° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula XII.

In some embodiments, about 1.0 to about 2.0 equivalents of the compound of Formula XXI is used based on 1 equivalent of the compound of Formula XII.

In some embodiments, the compound of Formula XII is prepared by a process comprising oxidizing a compound of Formula XIII:

wherein P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the oxidizing comprises adding a first oxidizing agent to the compound of Formula XIII to form a first mixture.

In some embodiments, the first oxidizing agent is 2,2,6,6-tetramethyl-1-piperidinyloxy free radical (TEMPO).

In some embodiments, the adding of said first oxidizing agent is conducted in the presence of tetra-N-butylammonium chloride.

In some embodiments, the adding of said first oxidizing agent is run at a temperature of about room temperature.

In some embodiments, the oxidizing further comprises adding a base and a second oxidizing agent to said first mixture.

In some embodiments, the second oxidizing agent is an N-halosuccinimide compound.

In some embodiments, the second oxidizing agent is N-chlorosuccinimide.

In some embodiments, the compound of Formula XIII is prepared by a process comprising reacting a compound of Formula XV:

with a compound of Formula XIV:

in the presence of boron trifluoride diethyl etherate and an eighth solvent component, wherein P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the eighth solvent component comprises acetone.

In some embodiments, the reacting is run at a temperature of about room temperature.

In some embodiments, the compound of Formula XV is prepared by a process comprising reacting a compound of Formula XVI:

in the presence of a reducing agent and a ninth solvent component, wherein P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the reducing agent is lithium borohydride.

In some embodiments, the reducing agent that is present in the reaction of the compound of Formula XVI is referred to as a first reducing agent.

In some embodiments, the ninth solvent component comprises tetrahydrofuran.

In some embodiments, the reacting is run at a temperature from about 0° C. to about 40° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula XVI.

In some embodiments, the compound of Formula VIII is prepared by a process comprising reacting a compound of Formula XVII:

with hydrogen gas in the presence of a hydrogenation catalyst and a tenth solvent component;

wherein P¹ is an amine protecting group.

The

group in Formula XVII indicates that the CN group can be E or Z relative to the oxygen of the pyran ring. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the hydrogenation catalyst is palladium on carbon.

In some embodiments, about 5 to about 15 weight % of the hydrogenation catalyst is used based on total mass of the compound of Formula XVII.

In some embodiments, the tenth solvent component comprises methanol.

In some embodiments, the compound of Formula XVII is prepared by

(i) reacting a compound of Formula XVIII:

with a Wittig reagent in the presence of an eleventh solvent component, wherein said Wittig reagent is prepared by a process comprising reacting a compound of Formula XXII:

with a strong base, wherein:

R^(a1), R^(b1), and R^(c1) are each independently C₁₋₆ alkyl;

Y⁻ is a halide ion; and

P¹ is an amine protecting group.

In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, Y⁻ is Cl⁻.

In some embodiments, R^(a1), R^(b1), and R^(c1) are each methyl.

In some embodiments, R^(a1), R^(b1), and R^(c1) are each n-butyl.

In some embodiments, the strong base is potassium tert-butoxide.

In some embodiments, the strong base is lithium hexamethyldisilazide.

In some embodiments, the strong base that is reacted with a compound of Formula XXII is referred to as a fourth strong base.

In some embodiments, the eleventh solvent component comprises tetrahydrofuran.

In some embodiments, the eleventh solvent component comprises N,N-dimethylacetamide.

In some embodiments, the eleventh solvent component comprises tetrahydrofuran and N,N-dimethylacetamide.

In some embodiments, the compound of Formula XVIII is formed by a process comprising reacting a compound of Formula XIX:

in the presence of a weak organic acid and a twelfth solvent component, wherein P¹ is an amine protecting group. In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the weak organic acid is acetic acid.

In some embodiments, the twelfth solvent component comprises toluene.

In some embodiments, the reacting is run at a temperature at reflux.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula XIX.

In some embodiments, the compound of Formula XIX is formed by a process comprising:

(i) reacting a compound of Formula XX:

with a compound of Formula XXIII:

in the presence of an amine base and an thirteenth solvent component to form a compound of Formula XXIV:

wherein

R^(a2) is C₁₋₄ alkoxy;

X¹ is halo; and

P¹ is an amine protecting group.

In some embodiments, P¹ is t-butoxycarbonyl.

In some embodiments, the compound of Formula XXIII is ethyl chloroformate.

In some embodiments, the amine base is N-methylmorpholine.

In some embodiments, the amine base that is present in the reaction of the compound of Formula XX is referred to as a second tertiary amine base.

In some embodiments, the thirteenth solvent component comprises tetrahydrofuran.

In some embodiments, the reacting is run at a temperature at about 0° C.

In some embodiments, the reacting step is referred to as the reacting of a compound of Formula XX.

In some embodiments, the process further comprises reducing said compound of Formula XXIV with a reducing agent.

In some embodiments, the reducing agent is sodium borohydride.

In some embodiments, the reducing agent is dissolved in a fourteenth solvent component.

In some embodiments, the reducing agent that is present in the reducing of the compound of Formula XXIV is referred to as a second reducing agent.

In some embodiments, the fourteenth solvent component comprises diglyme.

In some embodiments, the reducing is run at a temperature from about 70° C. to about 80° C.

In some embodiments, the reducing step is referred to as the reducing of a compound of Formula XXIV.

In some embodiments, the composition comprising a compound of Formula Ia and a compound of Formula Ib is prepared by a process comprising reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb:

with (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole:

or a salt thereof.

In some embodiments, the reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb is performed at a temperature from about 60° C. to about 70° C.

In some embodiments, the reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb is performed in the presence of a fifteenth solvent component.

In some embodiments, the fifteenth solvent component comprises methanol.

In some embodiments, the (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole is prepared by reacting (R)-2,2,5-trimethyloxazolidin-4-one:

with trimethyloxonium tetrafluoroborate.

In some embodiments, about 1 equivalent of trimethyloxonium tetrafluoroborate is used based on 1 equivalent of (R)-2,2,5-trimethyloxazolidin-4-one.

In some embodiments, the reacting of (R)-2,2,5-trimethyloxazolidin-4-one is performed at about room temperature.

In some embodiments, the reacting of (R)-2,2,5-trimethyloxazolidin-4-one is performed in the presence of a sixteenth solvent component.

In some embodiments, the sixteenth solvent component comprises anhydrous dichloromethane.

In some embodiments, the steps of reacting (R)-2,2,5-trimethyloxazolidin-4-one with trimethyloxonium tetrafluoroborate to form (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole and reacting (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole with a composition comprising a compound of Formula IIIa and a compound of Formula IIIb are conducted in the same pot without isolation of (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole.

In some embodiments, the composition comprising a compound of Formula Ia and a compound of Formula Ib is prepared by a process comprising reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb:

with (R)-ethyl 2-hydroxypropanimidate:

In some embodiments, the reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb is performed at a temperature from about 75° C. to about 85° C.

In some embodiments, the composition comprising a compound of Formula IIIa and a compound of Formula IIIb further comprises a seventeenth solvent component.

In some embodiments, the seventeenth solvent component comprises ethanol.

In some embodiments, prior to the reacting a composition comprising a compound of Formula IIIa and a compound of Formula IIIb, the (R)-ethyl 2-hydroxypropanimidate is dissolved in a eighteenth solvent component.

In some embodiments, the eighteenth solvent component comprises tetrahydrofuran.

In some embodiments, prior to the reacting the composition comprising a compound of Formula IIIa and a compound of Formula IIIb, the composition comprising a compound of Formula IIIa, a compound of Formula IIIb, and the seventeenth solvent component is heated at a temperature from about 75° C. to about 85° C.

In some embodiments, the (R)-ethyl 2-hydroxypropanimidate is prepared by reacting (R)-1-cyanoethyl acetate:

with ethanol in the presence of a strong acid.

In some embodiments, the strong acid used in the reaction of (R)-1-cyanoethyl acetate with ethanol is hydrogen chloride.

In some embodiments, about 2.9 to about 3.1 equivalents of ethanol is used based on 1 equivalent of (R)-ethyl 2-hydroxypropanimidate.

In some embodiments, the (R)-1-cyanoethyl acetate and ethanol are combined to form an ethanol mixture.

In some embodiments, the strong acid is added to the ethanol mixture to form a further mixture.

In some embodiments, the strong acid is added at a temperature from about −45° C. to about −35° C.

In some embodiments, adding the strong acid to the ethanol mixture to form a further mixture further comprises heating the further mixture to room temperature.

In some embodiments, the (R)-1-cyanoethyl acetate is formed by reacting (R)-1-amino-1-oxopropan-2-yl acetate:

with cyanuric chloride.

In some embodiments, about 0.4 to about 0.5 equivalents of cyanuric chloride is used based on 1 equivalent of (R)-1-amino-1-oxopropan-2-yl acetate.

In some embodiments, prior to the reacting of (R)-1-amino-1-oxopropan-2-yl acetate, the (R)-1-amino-1-oxopropan-2-yl acetate is mixed with a nineteenth solvent component.

In some embodiments, the nineteenth solvent component comprises N,N-dimethylformamide.

In some embodiments, prior to the reacting of (R)-1-amino-1-oxopropan-2-yl acetate, the cyanuric chloride is dissolved in a twentieth solvent component.

In some embodiments, the twentieth solvent component comprises 2-methoxy-2-methylpropane.

In some embodiments, the reacting of (R)-1-amino-1-oxopropan-2-yl acetate is performed at about room temperature.

In some embodiments, the (R)-1-amino-1-oxopropan-2-yl acetate is prepared by protecting (R)-2-hydroxypropanamide:

with acetyl chloride in the presence of an third tertiary amine base.

In some embodiments, the third tertiary amine base is 4-methylmorpholine.

In some embodiments, about 1 to about 1.1 equivalents of acetyl chloride is used based on 1 equivalent of (R)-2-hydroxypropanamide.

In some embodiments, the protecting is performed in the presence of a twenty-first solvent component.

In some embodiments, the twenty-first solvent component comprises tetrahydrofuran.

The present application further provides intermediates useful in the preparation of the compound of Formula Ia.

Accordingly, the present application provides a compound of Formula VIII:

wherein P¹ is an amine protecting group.

In some embodiments, P¹ is t-butoxycarbonyl.

The present application also provides a salt of Formula VIa:

The present application further provides a compound of Formula Va:

or salt thereof.

The present application further provides a compound of Formula Vb:

or salt thereof.

The present application further provides a compound of Formula IIIa:

or salt thereof.

The present application further provides a compound of Formula IIIb:

or salt thereof.

It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, can also be provided in combination in a single embodiment (while the embodiments are intended to be combined as if written in multiply dependent form). Conversely, various features of the invention which are, for brevity, described in the context of a single embodiment, can also be provided separately or in any suitable subcombination.

At various places in the present specification, substituents of compounds of the invention are disclosed in groups or in ranges. It is specifically intended that the invention include each and every individual subcombination of the members of such groups and ranges. For example, the term “C₁₋₆ alkyl” is specifically intended to individually disclose methyl, ethyl, C₃ alkyl, C₄ alkyl, C₅ alkyl, and C₆ alkyl.

As used here, the term “Wittig reagent” refers to a ylide formed by the reaction of a phosphonate compound of formula P(═O)(C₁₋₆ alkoxy)₂(C₁₋₆ alkyl-CN), wherein the alkoxy and alkyl groups each have 1 to 6 carbons, in the presence of a strong base (e.g., potassium tert-butoxide). In some embodiments, the term “Wittig reagent” refers a ylide formed by the reaction of a phosphonium salt (e.g., cyanomethyl (trimethyl)phosphonium chloride or tributyl(cyanomethyl)phosphonium chloride) in the presence of a strong base (e.g., potassium tert-butoxide).

As used herein, the term “C_(n-m) alkyl”, employed alone or in combination with other terms, refers to a saturated hydrocarbon group that may be straight-chain or branched, having n to m carbon atoms. In some embodiments, the alkyl group contains 1 to 6, 1 to 4 or 1 to 3 carbon atoms. Examples of alkyl moieties include, but are not limited to, chemical groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, 2-methyl-1-butyl, 3-pentyl, n-hexyl, 1,2,2-trimethylpropyl, and the like.

As used herein, the term “C₁₋₆ alkoxy”, employed alone or in combination with other terms, refers to a group of formula —O-alkyl, wherein the alkyl group has 1 to 6 carbons. Example alkoxy groups include methoxy, ethoxy, propoxy (e.g., n-propoxy and isopropoxy), butoxy (e.g., n-butoxy, tert-butoxy), and the like.

As used herein, the term “C₁₋₆ alkyloxonium reagent” refers to a reagent having a cation of group of formula (C₁₋₆ alkyl)₃O⁺, wherein the C₁₋₆ alkyl group refers to a linear or branched alkyl group having 1 to 6 carbons. Example C₁₋₆ alkyloxonium reagents include trimethyloxonium tetrafluoroborate, triethyloxonium tetrafluoroborate (Meerwein's reagent), triethyloxonium hexafluorophosphate, triethyloxonium hexachloroantimonate, and the like. Counter ions include, but are not limited to tetrafluoroborate, hexafluorophosphate, and hexachloroantimonate.

As used herein, the term “amino” refers to a group of formula —NH₂.

As used herein, the term “amine base” refers to a mono-substituted amine group (i.e., primary amine base), di-substituted amine group (i.e., secondary amine base), or a tri-substituted amine group (i.e., tertiary amine base). Example mono-substituted amine bases include methyl amine, ethyl amine, propyl amine, butyl amine, and the like. Example di-substituted amine bases include dimethylamine, diethylamine, dipropylamine, dibutylamine, pyrrolidine, piperidine, azepane, morpholine, and the like. In some embodiments, the tertiary amine has the formula N(R′)3, wherein each R′ is independently C₁₋₆ alkyl, 3-10 member cycloalkyl, 4-10 membered heterocycloalkyl, 1-10 membered heteroaryl, and 5-10 membered aryl, wherein said 3-10 member cycloalkyl, 4-10 membered heterocycloalkyl, 1-10 membered heteroaryl, and 5-10 membered aryl are optionally substituted by 1, 2, 3, 4, 5, or 6 C₁₋₆ alkyl groups. Example tertiary amine bases include trimethylamine, triethylamine, tripropylamine, triisopropylamine, tributylamine, tri-tert-butylamine, N,N-dimethylethanamine, N-ethyl-N-methylpropan-2-amine, N-ethyl-N-isopropylpropan-2-amine, N-methylmorpholine, and the like. In some embodiments, the term “tertiary amine base” refers to a group of formula N(R)₃, wherein each R is independently a linear or branched C₁₋₆ alkyl group.

As used herein, the term “cycloalkyl”, employed alone or in combination with other terms, refers to a non-aromatic cyclic hydrocarbon moiety, which may optionally contain one or more alkenylene groups as part of the ring structure. In some embodiments, cycloalkyl is a 3-10 membered cycloalkyl, which is monocyclic or bicyclic. In some embodiments, cycloalkyl is a 3-6 or 3-7 monocyclic cycloalkyl. Exemplary cycloalkyl groups include 1,2,3,4-tetrahydro-naphthalene, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptatrienyl, norbornyl, norpinyl, norcaranyl, adamantyl, and the like. In some embodiments, the cycloalkyl group is cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.

As used herein, the term “aryl”, employed alone or in combination with other terms, refers to a monocyclic or polycyclic (e.g., having 2, 3 or 4 fused rings) aromatic hydrocarbon, such as, but not limited to, phenyl, 1-naphthyl, 2-naphthyl, anthracenyl, phenanthrenyl, and the like. In some embodiments, aryl is C₆₋₁₀ aryl. In some embodiments, the aryl group is a naphthalene ring or phenyl ring. In some embodiments, the aryl group is phenyl.

As used herein, the term “heteroaryl”, employed alone or in combination with other terms, refers to a monocyclic or polycyclic (e.g., having 2, 3 or 4 fused rings) aromatic hydrocarbon moiety, having one or more heteroatom ring members selected from nitrogen, sulfur and oxygen. In some embodiments, heteroaryl is a 5-10 membered heteroaryl, which is monocyclic or bicyclic, comprising 1 to 9 carbon atoms and 1, 2, 3, or 4 heteroatom ring members independently selected from nitrogen, sulfur and oxygen. Example heteroaryl groups include, but are not limited to, pyridine, pyrimidine, pyrazine, pyridazine, pyrrole, pyrazole, azolyl, oxazole, thiazole, imidazole, furan, thiophene, quinoline, isoquinoline, indole, benzothiophene, benzofuran, benzisoxazole, imidazo[1,2-b]thiazole, purine, or the like.

As used herein, the term “heterocycloalkyl”, employed alone or in combination with other terms, refers to non-aromatic ring system, which may optionally contain one or more alkenylene or alkynylene groups as part of the ring structure, and which has at least one heteroatom ring member independently selected from nitrogen, sulfur and oxygen. When the heterocycloalkyl groups contains more than one heteroatom, the heteroatoms may be the same or different. Heterocycloalkyl groups can include mono- or polycyclic (e.g., having 2, 3 or 4 fused, spirocyclic, or bridged rings) ring systems. In some embodiments, heterocycloalkyl is 5-10 membered heterocycloalkyl, which is monocyclic or bicyclic, comprising 2 to 9 carbon atoms and 1, 2, 3, or 4 heteroatom ring members independently selected from nitrogen, sulfur, and oxygen. Examples of heterocycloalkyl groups include 1,2,3,4-tetrahydro-quinoline, azetidine, azepane, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, pyran, and a 2-oxo-1,3-oxazolidine ring.

As used herein, the term “alkali metal” includes lithium, sodium, and potassium.

As used herein, “halo” or “halogen”, employed alone or in combination with other terms, includes fluoro, chloro, bromo, and iodo.

Example “N-halosuccinimide compound” include, but are not limited to, N-chlorosuccinimide, N-bromosuccinimide, and N-iodosuccinimide.

As used herein, the term “alkoxide base” refers to a base having a group of formula (C₁₋₆ alkyl)O⁻, wherein the C₁₋₆ alkyl refers to a linear or branched alkyl group having 1 to 6 carbons. Example alkoxide bases include, but are not limited to, methoxide, ethoxide, propoxide, isopropoxide, n-butoxide, iso-butoxide, tert-butoxide, and the like.

As used herein, the term “alkali metal alkoxide” refers to a group of formula M(O—C₁₋₆ alkyl), wherein M refers to an alkali metal (e.g., lithium, sodium, or potassium) and C₁₋₆ alkyl refers to a linear or branched alkyl group having 1 to 6 carbons. Example alkali metal alkoxides include, but are not limited to, sodium methoxide, sodium ethoxide, sodium isopropoxide, sodium tert-butoxide, lithium methoxide, lithium ethoxide, potassium methoxide, potassium ethoxide, potassium tert-butoxide, and the like.

As used herein the term, “hydrogenation catalyst” refers to a metal (e.g., palladium, nickel, or rhodium) catalyst suitable to catalyze a hydrogenation reaction (i.e., reaction of a compound with hydrogen gas). Example hydrogenation catalysts include, but are not limited to, palladium on carbon, Lindlar's catalyst (palladium deposited on calcium carbonate or barium sulfate), Wilkinson's catalyst, HRuCl(PPh₃)₃, RhCl(PPh₃)₃, [Rh(COD)Cl]₂, [Ir(COD)(PMePh₂)₂]⁺, [Rh(1,5-cyclooctadiene)(PPh₃)₂]⁺, PtO₂ (Adam's catalyst), palladium on carbon, palladium black, Lindlar's catalyst (palladium deposited on calcium carbonate or barium sulfate and treated with lead), and the like. In some embodiments, the hydrogenation catalyst is one found in Nishimura, Heterogeneous Catalytic Hydrogenation for Organic Synthesis, Edition 1, Wiley (Apr. 17, 2001) or Chaloner, Homogeneous Hydrogenation, Edition 1, Springer Netherlands (Dec. 6, 2010), each of which is incorporated herein by reference in its entirety.

Appropriate P¹ protecting groups include, but are not limited to the protecting groups for amines delineated in Wuts and Greene, Protective Groups in Organic Synthesis, 4th ed., John Wiley & Sons: New Jersey, pages 696-887 (and, in particular, pages 872-887) (2007), which is incorporated herein by reference in its entirety. Example amine protecting groups include, but are not limited to, benzyloxycarbonyl (Cbz), 2,2,2-trichloroethoxycarbonyl (Troc), 2-(trimethylsilyl)ethoxycarbonyl (Teoc), 2-(4-trifluoromethylphenylsulfonyl)ethoxycarbonyl (Tsc), t-butoxycarbonyl (BOC), 1-adamantyloxycarbonyl (Adoc), 2-adamantylcarbonyl (2-Adoc), 2,4-dimethylpent-3-yloxycarbonyl (Doc), cyclohexyloxycarbonyl (Hoc), 1,1-dimethyl-2,2,2-trichloroethoxycarbonyl (TcBOC), vinyl, 2-chloroethyl, 2-phenylsulfonylethyl, allyl, benzyl, 2-nitrobenzyl, 4-nitrobenzyl, diphenyl-4-pyridylmethyl, N′,N′-dimethylhydrazinyl, methoxymethyl, t-butoxymethyl (Bum), benzyloxymethyl (BOM), or 2-tetrahydropyranyl (THP), tri(C₁₋₄ alkyl)silyl (e.g., tri(isopropyl)silyl), 1,1-diethoxymethyl, or N-pivaloyloxymethyl (POM).

Example oxidizing agents include Dess-Martin periodinane, 2,2,6,6-tetramethyl-1-piperidinyloxy free radical (TEMPO), N-halosuccinimide (e.g., N-bromosuccinimide, N-chlorosuccinimide, N-iodosuccinimide), and the like.

Example reducing agents include alkali metal borohydrides (e.g., lithium borohydride, sodium borohydride, potassium borohydride, etc.), alkali metal aluminum hydrides (e.g., lithium aluminum hydride, sodium aluminum hydride), hydrogen gas (e.g., H₂/Pd on carbon), and the like.

Example acids can be inorganic or organic acids and include, but are not limited to, strong and weak acids. Some example acids include hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 4-nitrobenzoic acid, methanesulfonic acid, benzenesulfonic acid, trifluoroacetic acid, and nitric acid. Some weak acids include, but are not limited to acetic acid, propionic acid, butanoic acid, benzoic acid, tartaric acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, and decanoic acid.

Some example strong bases include, but are not limited to, hydroxide, alkoxides, metal amides, metal hydrides, metal dialkylamides and arylamines, wherein; alkoxides include lithium, sodium and potassium salts of methyl, ethyl and t butyl oxides; metal amides include sodium amide, potassium amide and lithium amide; metal hydrides include sodium hydride, potassium hydride and lithium hydride; and metal dialkylamides include lithium, sodium, and potassium salts of methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl, trimethylsilyl and cyclohexyl substituted amides.

All compounds, and pharmaceutically acceptable salts thereof, can be found together with other substances such as water and solvents (e.g., hydrates and solvates) or can be isolated.

In some embodiments, the compounds of the invention, or salts thereof, are substantially isolated. By “substantially isolated” is meant that the compound is at least partially or substantially separated from the environment in which it was formed or detected. Partial separation can include, for example, a composition enriched in the compounds of the invention. Substantial separation can include compositions containing at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, or at least about 99% by weight of the compounds of the invention, or salt thereof. Methods for isolating compounds and their salts are routine in the art.

As used herein, the term “reacting” is used as known in the art and generally refers to the bringing together of chemical reagents in such a manner so as to allow their interaction at the molecular level to achieve a chemical or physical transformation. In some embodiments, the reacting involves two reagents, wherein one or more equivalents of second reagent are used with respect to the first reagent. The reacting steps of the processes described herein can be conducted for a time and under conditions suitable for preparing the identified product.

The reactions of the processes described herein can be carried out in suitable solvents which can be readily selected by one of skill in the art of organic synthesis. Suitable solvents can be substantially nonreactive with the starting materials (reactants), the intermediates, or products at the temperatures at which the reactions are carried out, e.g., temperatures which can range from the solvent's freezing temperature to the solvent's boiling temperature. A given reaction can be carried out in one solvent or a mixture of more than one solvent. Depending on the particular reaction step, suitable solvents for a particular reaction step can be selected. In some embodiments, reactions can be carried out in the absence of solvent, such as when at least one of the reagents is a liquid or gas.

A “solvent component” may be one solvent or a mixture of two or more solvents.

As used herein, “second”, “third,” “fourth”, etc. as a prefix to the phrase “solvent component” is used to differentiate the solvent component from other solvent components used in earlier or later steps of the process and does not indicate that multiple solvents must be present.

Suitable solvents can include halogenated solvents such as carbon tetrachloride, bromodichloromethane, dibromochloromethane, bromoform, chloroform, bromochloromethane, dibromomethane, butyl chloride, dichloromethane, tetrachloroethylene, trichloroethylene, 1,1,1-trichloroethane, 1,1,2-trichloroethane, 1,1-dichloro ethane, 2-chloropropane, α,α,α-trifluorotoluene, 1,2-dichloroethane, 1,2-dibromoethane, hexafluorobenzene, 1,2,4-trichlorobenzene, 1,2-dichlorobenzene, chlorobenzene, fluorobenzene, mixtures thereof and the like.

Suitable ether solvents include: dimethoxymethane, tetrahydrofuran, 1,3-dioxane, 1,4-dioxane, furan, diethyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether (diglyme), diethylene glycol diethyl ether, triethylene glycol dimethyl ether, anisole, t-butyl methyl ether, mixtures thereof and the like.

Suitable protic solvents can include, by way of example and without limitation, water, methanol, ethanol, 2-nitroethanol, 2-fluoroethanol, 2,2,2-trifluoroethanol, ethylene glycol, 1-propanol, 2-propanol, 2-methoxyethanol, 1-butanol, 2-butanol, i-butyl alcohol, t-butyl alcohol, 2-ethoxyethanol, diethylene glycol, 1-, 2-, or 3-pentanol, neo-pentyl alcohol, t-pentyl alcohol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, cyclohexanol, benzyl alcohol, phenol, or glycerol.

Suitable aprotic solvents can include, by way of example and without limitation, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU), 1,3-dimethyl-2-imidazolidinone (DMI), N-methylpyrrolidinone (NMP), formamide, N-methylacetamide, N-methylformamide, acetonitrile, dimethyl sulfoxide, propionitrile, ethyl formate, methyl acetate, hexachloroacetone, acetone, ethyl methyl ketone, ethyl acetate, sulfolane, N,N-dimethylpropionamide, tetramethylurea, nitromethane, nitrobenzene, or hexamethylphosphoramide.

Suitable hydrocarbon solvents include benzene, cyclohexane, pentane, hexane, toluene, cycloheptane, methylcyclohexane, heptane, ethylbenzene, m-, o-, or p-xylene, octane, indane, nonane, or naphthalene.

The reactions of the processes described herein can be carried out in air or under an inert atmosphere. Typically, reactions containing reagents or products that are substantially reactive with air can be carried out using air-sensitive synthetic techniques that are well known to the skilled artisan.

In some embodiments, preparation of compounds can involve the addition of acids or bases to affect, for example, catalysis of a desired reaction or formation of salt forms such as acid addition salts.

Example acids can be inorganic or organic acids. Inorganic acids include hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, and nitric acid. Organic acids include formic acid, acetic acid, propionic acid, butanoic acid, benzoic acid, 4-nitrobenzoic acid, methanesulfonic acid, p-toluenesulfonic acid, benzenesulfonic acid, tartaric acid, trifluoroacetic acid, propiolic acid, butyric acid, 2-butynoic acid, vinyl acetic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid and decanoic acid.

Example bases include lithium hydroxide, sodium hydroxide, potassium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate, and sodium bicarbonate. Some example strong bases include, but are not limited to, hydroxide, alkoxides, metal amides, metal hydrides, metal dialkylamides and arylamines, wherein; alkoxides include lithium, sodium and potassium salts of methyl, ethyl and t-butyl oxides; metal amides include sodium amide, potassium amide and lithium amide; metal hydrides include sodium hydride, potassium hydride and lithium hydride; and metal dialkylamides include lithium, sodium, and potassium salts of methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl, trimethylsilyl and cyclohexyl substituted amides.

Upon carrying out preparation of compounds according to the processes described herein, the usual isolation and purification operations such as concentration, filtration, extraction, solid-phase extraction, recrystallization, chromatography, and the like may be used, to isolate the desired products.

The expression, “room temperature,” as used herein, is understood in the art, and refer generally to a temperature (e.g. a reaction temperature) that is about the temperature of the room in which the reaction is carried out, for example, a temperature from about 20° C. to about 30° C.

The reactions of the processes described herein can be carried out at appropriate temperatures which can be readily determined by the skilled artisan. Reaction temperatures will depend on, for example, the melting and boiling points of the reagents and solvent, if present; the thermodynamics of the reaction (e.g., vigorously exothermic reactions may need to be carried out at reduced temperatures); and the kinetics of the reaction (e.g., a high activation energy barrier may need elevated temperatures).

Preparation of the compounds described herein can involve the protection and deprotection of various chemical groups (e.g, protection and deprotection of amine groups). The need for protection and deprotection, and the selection of appropriate protecting groups, can be readily determined by one skilled in the art. The chemistry of protecting groups can be found, for example, in Wuts and Greene, Protective Groups in Organic Synthesis, 4th ed., John Wiley & Sons: New Jersey, (2007), which is incorporated herein by reference in its entirety. Adjustments to the protecting groups and formation and cleavage methods described herein may be adjusted as necessary in light of the various substituents.

As used herein, the term “deprotection conditions” refers to conditions suitable to cleave an amine protecting group. In some embodiments, deprotection conditions may include cleavage of a protecting group in the presence of a strong acid, in the presence of a strong base, in the presence of a reducing agent, or in the presence of an oxidizing agent. Deprotection of an amine protecting group can be accomplished by methods known in the art for the removal of particular protecting groups for amines, such as those in Wuts and Greene, Protective Groups in Organic Synthesis, 4th ed., John Wiley & Sons: New Jersey, pages 696-887 (and, in particular, pages 872-887) (2007), which is incorporated herein by reference in its entirety. In some embodiments, the treating comprises reacting the protected compound under acidic conditions (e.g., hydrochloric acid or trifluoroacetic acid). In some embodiments, the temperature is about room temperature, at a temperature from about 15° C. to about 40° C., or at a temperature from about 15° C. to about 30° C.

Reactions can be monitored according to any suitable method known in the art. For example, product formation can be monitored by spectroscopic means, such as nuclear magnetic resonance spectroscopy (e.g., ¹H or ¹³C), infrared spectroscopy, spectrophotometry (e.g., UV-visible), mass spectrometry, or by chromatographic methods such as high performance liquid chromatography (HPLC) or thin layer chromatography (TLC).

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

The present invention also includes pharmaceutically acceptable salts of the compounds described herein. As used herein, “pharmaceutically acceptable salts” refers to derivatives of the disclosed compounds wherein the parent compound is modified by converting an existing acid or base moiety to its salt form. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts of the present invention include the non-toxic salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, non-aqueous media like ether, ethyl acetate, alcohols (e.g., methanol, ethanol, iso-propanol, or butanol) or acetonitrile (ACN) are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418 and Journal of Pharmaceutical Science, 66, 2 (1977), each of which is incorporated herein by reference in its entirety. In some embodiments, the compounds described herein include the N-oxide forms.

Methods

The compound of Formula Ia, 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, is a selective inhibitor of JAK1. The compound of Formula Ia inhibits JAK1 preferentially over JAK2 (e.g., have a JAK1/JAK2 IC₅₀ ratio >10).

JAK1 plays a central role in a number of cytokine and growth factor signaling pathways that, when dysregulated, can result in or contribute to disease states. For example, IL-6 levels are elevated in rheumatoid arthritis, a disease in which it has been suggested to have detrimental effects (Fonesca, J. E. et al., Autoimmunity Reviews, 8:538-42, 2009). Because IL-6 signals, at least in part, through JAK1, antagonizing IL-6 directly or indirectly through JAK1 inhibition is expected to provide clinical benefit (Guschin, D., N., et al Embo J 14:1421, 1995; Smolen, J. S., et al. Lancet 371:987, 2008). Moreover, in some cancers JAK1 is mutated resulting in constitutive undesirable tumor cell growth and survival (Mullighan C G, Proc Natl Acad Sci USA. 106:9414-8, 2009; Flex E., et al. J Exp Med. 205:751-8, 2008). In other autoimmune diseases and cancers elevated systemic levels of inflammatory cytokines that activate JAK1 may also contribute to the disease and/or associated symptoms. Therefore, patients with such diseases may benefit from JAK1 inhibition. Selective inhibitors of JAK1 may be efficacious while avoiding unnecessary and potentially undesirable effects of inhibiting other JAK kinases.

Selective inhibitors of JAK1, relative to other JAK kinases, may have multiple therapeutic advantages over less selective inhibitors. With respect to selectivity against JAK2, a number of important cytokines and growth factors signal through JAK2 including, for example, erythropoietin (Epo) and thrombopoietin (Tpo) (Parganas E, et al. Cell. 93:385-95, 1998). Epo is a key growth factor for red blood cells production; hence a paucity of Epo-dependent signaling can result in reduced numbers of red blood cells and anemia (Kaushansky K, NEJM 354:2034-45, 2006). Tpo, another example of a JAK2-dependent growth factor, plays a central role in controlling the proliferation and maturation of megakaryocytes—the cells from which platelets are produced (Kaushansky K, NEJM 354:2034-45, 2006). As such, reduced Tpo signaling would decrease megakaryocyte numbers (megakaryocytopenia) and lower circulating platelet counts (thrombocytopenia). This can result in undesirable and/or uncontrollable bleeding. Reduced inhibition of other JAKs, such as JAK3 and Tyk2, may also be desirable as humans lacking functional version of these kinases have been shown to suffer from numerous maladies such as severe-combined immunodeficiency or hyperimmunoglobulin E syndrome (Minegishi, Y, et al. Immunity 25:745-55, 2006; Macchi P, et al. Nature. 377:65-8, 1995). Therefore a JAK1 inhibitor with reduced affinity for other JAKs would have significant advantages over a less-selective inhibitor with respect to reduced side effects involving immune suppression, anemia and thrombocytopenia.

Another aspect of the present invention pertains to methods of treating a JAK-associated disease or disorder in an individual (e.g., patient) by administering to the individual in need of such treatment a therapeutically effective amount or dose of a compound of the present invention or a pharmaceutical composition thereof. A JAK-associated disease can include any disease, disorder or condition that is directly or indirectly linked to expression or activity of the JAK, including overexpression and/or abnormal activity levels. A JAK-associated disease can also include any disease, disorder or condition that can be prevented, ameliorated, or cured by modulating JAK activity.

JAK inhibitors are useful in treating various JAK-associated diseases or disorders. Examples of JAK-associated diseases include diseases involving the immune system including, for example, organ transplant rejection (e.g., allograft rejection and graft versus host disease). Further examples of JAK-associated diseases include autoimmune diseases such as multiple sclerosis, rheumatoid arthritis, juvenile arthritis, psoriatic arthritis, type I diabetes, lupus, psoriasis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, myasthenia gravis, immunoglobulin nephropathies, myocarditis, autoimmune thyroid disorders, chronic obstructive pulmonary disease (COPD), and the like. In some embodiments, the autoimmune disease is an autoimmune bullous skin disorder such as pemphigus vulgaris (PV) or bullous pemphigoid (BP).

Further examples of JAK-associated diseases include allergic conditions such as asthma, food allergies, eszematous dermatitis, contact dermatitis, atopic dermatitis (atropic eczema), and rhinitis. Further examples of JAK-associated diseases include viral diseases such as Epstein Barr Virus (EBV), Hepatitis B, Hepatitis C, HIV, HTLV 1, Varicella-Zoster Virus (VZV) and Human Papilloma Virus (HPV).

Further examples of JAK-associated diseases include diseases associated with cartilage turnover, for example, gouty arthritis, septic or infectious arthritis, reactive arthritis, reflex sympathetic dystrophy, algodystrophy, Tietze syndrome, costal athropathy, osteoarthritis deformans endemica, Mseleni disease, Handigodu disease, degeneration resulting from fibromyalgia, systemic lupus erythematosus, scleroderma, or ankylosing spondylitis.

Further examples of JAK-associated disease include congenital cartilage malformations, including hereditary chrondrolysis, chrondrodysplasias, and pseudochrondrodysplasias (e.g., microtia, enotia, and metaphyseal chrondrodysplasia).

Further examples of JAK-associated diseases or conditions include skin disorders such as psoriasis (for example, psoriasis vulgaris), atopic dermatitis, skin rash, skin irritation, skin sensitization (e.g., contact dermatitis or allergic contact dermatitis). For example, certain substances including some pharmaceuticals when topically applied can cause skin sensitization. In some embodiments, co-administration or sequential administration of at least one JAK inhibitor of the invention together with the agent causing unwanted sensitization can be helpful in treating such unwanted sensitization or dermatitis. In some embodiments, the skin disorder is treated by topical administration of at least one JAK inhibitor of the invention.

Further examples of JAK-associated diseases or conditions include those characterized by solid tumors (e.g., prostate cancer, renal cancer, hepatic cancer, pancreatic cancer, gastric cancer, breast cancer, lung cancer, cancers of the head and neck, thyroid cancer, glioblastoma, Kaposi's sarcoma, Castleman's disease, uterine leiomyosarcoma, melanoma etc.), hematological cancers (e.g., lymphoma, leukemia such as acute lymphoblastic leukemia (ALL), acute myelogenous leukemia (AML) or multiple myeloma), and skin cancer such as cutaneous T-cell lymphoma (CTCL) and cutaneous B-cell lymphoma. Example CTCLs include Sezary syndrome and mycosis fungoides. Other examples of JAK-associated diseases or conditions include pulmonary arterial hypertension.

Other examples of JAK-associated diseases or conditions include inflammation-associated cancers. In some embodiments, the cancer is associated with inflammatory bowel disease. In some embodiments, the inflammatory bowel disease is ulcerative colitis. In some embodiments, the inflammatory bowel disease is Crohn's disease. In some embodiments, the inflammation-associated cancer is colitis-associated cancer. In some embodiments, the inflammation-associated cancer is colon cancer or colorectal cancer. In some embodiments, the cancer is gastric cancer, gastrointestinal carcinoid tumor, gastrointestinal stromal tumor (GIST), adenocarcinoma, small intestine cancer, or rectal cancer.

JAK-associated diseases can further include those characterized by expression of: JAK2 mutants such as those having at least one mutation in the pseudo-kinase domain (e.g., JAK2V617F); JAK2 mutants having at least one mutation outside of the pseudo-kinase domain; JAK1 mutants; JAK3 mutants; erythropoietin receptor (EPOR) mutants; or deregulated expression of CRLF2.

JAK-associated diseases can further include myeloproliferative disorders (MPDs) such as polycythemia vera (PV), essential thrombocythemia (ET), myelofibrosis with myeloid metaplasia (MMM), primary myelofibrosis (PMF), chronic myelogenous leukemia (CML), chronic myelomonocytic leukemia (CMML), hypereosinophilic syndrome (HES), systemic mast cell disease (SMCD), and the like. In some embodiments, the myeloproliferative disorder is myelofibrosis (e.g., primary myelofibrosis (PMF) or post polycythemia vera/essential thrombocythemia myelofibrosis (Post-PV/Post-ET MF)). In some embodiments, the myeloproliferative disorder is post-essential thrombocythemia myelofibrosis (Post-ET MF). In some embodiments, the myeloproliferative disorder is post polycythemia vera myelofibrosis (Post-PV MF).

JAK-associated diseases further include myelodysplastic syndrome (MDS).

As used herein, myelodysplastic syndromes are intended to encompass heterogeneous and clonal hematopoietic disorders that are characterized by ineffective hematopoiesis on one or more of the major myeloid cell lineages. Myelodysplastic syndromes are associated with bone marrow failure, peripheral blood cytopenias, and a propensity to progress to acute myeloid leukemia (AML). Moreover, clonal cytogenetic abnormalities can be detected in about 50% of cases with MDS. In 1997, The World Health Organization (WHO) in conjunction with the Society for Hematopathology (SH) and the European Association of Hematopathology (EAHP) proposed new classifications for hematopoietic neoplasms (Harris, et al., J Clin Oncol 1999; 17:3835-3849; Vardiman, et al., Blood 2002; 100:2292-2302). For MDS, the WHO utilized not only the morphologic criteria from the French-American-British (FAB) classification but also incorporated available genetic, biologic, and clinical characteristics to define subsets of MDS (Bennett, et al., Br J Haematol 1982; 51:189-199). In 2008, the WHO classification of MDS (Table 1) was further refined to allow precise and prognostically relevant subclassification of unilineage dysplasia by incorporating new clinical and scientific information (Vardiman, et al., Blood 2009; 114:937-951; Swerdlow, et al., WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th Edition. Lyon France: IARC Press; 2008:88-103; Bunning and Germing, “Myelodysplastic syndromes/neoplasms” in Chapter 5, Swerdlow, et al, eds. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. (ed. 4th edition): Lyon, France: IARC Press; 2008:88-103).

TABLE 1 2008 WHO Classification for De Novo Myelodysplastic Syndrome Subtype Blood Bone Marrow Refractory cytopenia with Single or Bicytopenia Dysplasia in ≥10% of 1 cell unilineage dysplasia line, <5% blasts (RCUD) Refractory anemia with ring Anemia, no blasts ≥15% of erythroid precursors sideroblasts (RARS) w/ring sideroblasts, erythroid dysplasia only, <5% blasts Refractory cytopenia with Cytopenia(s), <1 × 10⁹/L Dysplasia in ≥10% of cells multilineage dysplasia monocytes in ≥2 hematopoietic lineages, ±15% ring sideroblasts, <5% blasts Refractory anemia with Cytopenia(s), ≤2% to 4% Unilineage or multilineage excess blasts-1 (RAEB-1) blasts, <1 × 10⁹/L dysplasia, No Auer rods, 5% to monocytes 9% blasts Refractory anemia with Cytopenia(s), ≤5% to Unilineage or multilineage excess blasts-2 (RAEB-2) 19% blasts, <1 × 10⁹/L dysplasia, ±Auer rods, 10% to monocytes 19% blasts Myelodysplastic syndrome, Cytopenias Unilineage or no dysplasia but unclassified (MDS-U) characteristic MDS cytogenetics, <5% blasts MDS associated with Anemia, platelets normal Unilineage erythroid. Isolated isolated del(5q) or increased del(5q), <5% blasts

In some embodiments, the present application provides a method of treating a myelodysplastic syndrome (MDS) in patient in need thereof, comprising administering to said patient a compound of Formula Ia, or a pharmaceutically acceptable salt thereof, wherein said MDS is selected from refractory cytopenia with unilineage dysplasia (RCUD), refractory anemia with ring sideroblasts (RARS), refractory cytopenia with multilineage dysplasia, refractory anemia with excess blasts-1 (RAEB-1), refractory anemia with excess blasts-2 (RAEB-2), myelodysplastic syndrome, unclassified (MDS-U), and MDS associated with isolated del(5q).

In some embodiments, the myelodysplastic syndrome is refractory cytopenia with unilineage dysplasia (RCUD).

In some embodiments, the myelodysplastic syndrome is refractory anemia with ring sideroblasts (RARS).

In some embodiments, the myelodysplastic syndrome is refractory cytopenia with multilineage dysplasia.

In some embodiments, the myelodysplastic syndrome is refractory anemia with excess blasts-1 (RAEB-1).

In some embodiments, the myelodysplastic syndrome is refractory anemia with excess blasts-2 (RAEB-2).

In some embodiments, the myelodysplastic syndrome is myelodysplastic syndrome, unclassified (MDS-U).

In some embodiments, the myelodysplastic syndrome is myelodysplastic syndrome associated with isolated del(5q).

In some embodiments, the myelodysplastic syndrome is refractory to erythropoiesis-stimulating agents.

Other examples of JAK-associated diseases or conditions include ameliorating the dermatological side effects of other pharmaceuticals by administration of the compound of the invention. For example, numerous pharmaceutical agents result in unwanted allergic reactions which can manifest as acneiform rash or related dermatitis. Example pharmaceutical agents that have such undesirable side effects include anti-cancer drugs such as gefitinib, cetuximab, erlotinib, and the like. The compounds of the invention can be administered systemically or topically (e.g., localized to the vicinity of the dermatitis) in combination with (e.g., simultaneously or sequentially) the pharmaceutical agent having the undesirable dermatological side effect. In some embodiments, the compound of the invention can be administered topically together with one or more other pharmaceuticals, where the other pharmaceuticals when topically applied in the absence of a compound of the invention cause contact dermatitis, allergic contact sensitization, or similar skin disorder. Accordingly, compositions of the invention include topical formulations containing the compound of the invention and a further pharmaceutical agent which can cause dermatitis, skin disorders, or related side effects.

Further JAK-associated diseases include inflammation and inflammatory diseases. Example inflammatory diseases include sarcoidosis, inflammatory diseases of the eye (e.g., iritis, uveitis, scleritis, conjunctivitis, or related disease), inflammatory diseases of the respiratory tract (e.g., the upper respiratory tract including the nose and sinuses such as rhinitis or sinusitis or the lower respiratory tract including bronchitis, chronic obstructive pulmonary disease, and the like), inflammatory myopathy such as myocarditis, and other inflammatory diseases. In some embodiments, the inflammation disease of the eye is blepharitis.

Further JAK-associated diseases include ischemia reperfusion injuries or a disease or condition related to an inflammatory ischemic event such as stroke or cardiac arrest, endotoxin-driven disease state (e.g., complications after bypass surgery or chronic endotoxin states contributing to chronic cardiac failure), anorexia, cachexia, fatigue such as that resulting from or associated with cancer, restenosis, sclerodermitis, fibrosis, conditions associated with hypoxia or astrogliosis such as, for example, diabetic retinopathy, cancer, or neurodegeneration, and other inflammatory diseases such as systemic inflammatory response syndrome (SIRS) and septic shock.

Other JAK-associated diseases include gout and increased prostate size due to, e.g., benign prostatic hypertrophy or benign prostatic hyperplasia, as well as bone resorption diseases such as osteoporosis or osteoarthritis, bone resorption diseases associated with: hormonal imbalance and/or hormonal therapy, autoimmune disease (e.g. osseous sarcoidosis), or cancer (e.g. myeloma).

Further JAK-associated diseases include a dry eye disorder. As used herein, “dry eye disorder” is intended to encompass the disease states summarized in a recent official report of the Dry Eye Workshop (DEWS), which defined dry eye as “a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface.” Lemp, “The Definition and Classification of Dry Eye Disease: Report of the Definition and Classification Subcommittee of the International Dry Eye Workshop”, The Ocular Surface, 5(2), 75-92 April 2007, which is incorporated herein by reference in its entirety. In some embodiments, the dry eye disorder is selected from aqueous tear-deficient dry eye (ADDE) or evaporative dry eye disorder, or appropriate combinations thereof. In some embodiments, the dry eye disorder is Sjogren syndrome dry eye (SSDE). In some embodiments, the dry eye disorder is non-Sjogren syndrome dry eye (NSSDE).

Further JAK-associated diseases include conjunctivitis, uveitis (including chronic uveitis), chorioditis, retinitis, cyclitis, sclieritis, episcleritis, or iritis. Other JAK-associated diseases include respiratory dysfunction or failure associated wth viral infection, such as influenza and SARS.

Combination Therapies

One or more additional pharmaceutical agents such as, for example, chemotherapeutics, anti-inflammatory agents, steroids, immunosuppressants, as well as PI3Kδ, mTor, Bcr-Abl, Flt-3, RAF and FAK kinase inhibitors such as, for example, those described in WO 2006/056399, which is incorporated herein by reference in its entirety, or other agents can be used in combination with the compounds described herein for treatment of JAK-associated diseases, disorders or conditions. The one or more additional pharmaceutical agents can be administered to a patient simultaneously or sequentially.

Example chemotherapeutics include proteosome inhibitors (e.g., bortezomib), thalidomide, revlimid, and DNA-damaging agents such as melphalan, doxorubicin, cyclophosphamide, vincristine, etoposide, carmustine, and the like.

Example steroids include coriticosteroids such as dexamethasone or prednisone.

Example Bcr-Abl inhibitors include the compounds, and pharmaceutically acceptable salts thereof, of the genera and species disclosed in U.S. Pat. No. 5,521,184, WO 04/005281, and U.S. Ser. No. 60/578,491, all of which are incorporated herein by reference in their entirety.

Example suitable Flt-3 inhibitors include compounds, and their pharmaceutically acceptable salts, as disclosed in WO 03/037347, WO 03/099771, and WO 04/046120, all of which are incorporated herein by reference in their entirety.

Example suitable RAF inhibitors include compounds, and their pharmaceutically acceptable salts, as disclosed in WO 00/09495 and WO 05/028444, both of which are incorporated herein by reference in their entirety.

Example suitable FAK inhibitors include compounds, and their pharmaceutically acceptable salts, as disclosed in WO 04/080980, WO 04/056786, WO 03/024967, WO 01/064655, WO 00/053595, and WO 01/014402, all of which are incorporated herein by reference in their entirety.

In some embodiments, the additional pharmaceutical agent is selected from IMiDs, an anti-IL-6 agent, an anti-TNF-α agent, a hypomethylating agent, and a biologic response modifier (BRM).

Generally, a BRM is a substance made from living organisms to treat disease, which may occur naturally in the body or may be made in the laboratory. Examples of BRMs include IL-2, interferon, various types of colony-stimulating factors (CSF, GM-CSF, G-CSF), monoclonal antibodies such as abciximab, etanercept, infliximab, rituximab, trasturzumab, and high dose ascorbate.

In some embodiments, the anti-TNF-α agent is infliximab, and etanercept.

In some embodiments, the hypomethylating agent is a DNA methyltransferase inhibitor. In some embodiments, the DNA methyltransferase inhibitor is selected from 5 azacytidine and decitabine.

Generally, IMiDs are as immunomodulatory agents. In some embodiments, the IMiD is selected from thalidomide, lenalidomide, pomalidomide, CC-11006, and CC-10015.

In some embodiments, the additional pharmaceutical agent is selected from anti-thymocyte globulin, recombinant human granulocyte colony-stimulating factor (G CSF), granulocyte-monocyte CSF (GM-CSF), a erythropoiesis-stimulating agent (ESA), and cyclosporine.

In some embodiments, the additional pharmaceutical agent is an additional JAK inhibitor. In some embodiments, the additional JAK inhibitor is tofacitinib or ruxolitinib.

In some embodiments, one or more of the compounds of the invention can be used in combination with one or more other kinase inhibitors including imatinib, particularly for treating patients resistant to imatinib or other kinase inhibitors.

In some embodiments, a suitable chemotherapeutical agent can be selected from antimetabolite agents, topoisomerase 1 inhibitors, platinum analogs, taxanes, anthracyclines, and EGFR inhibitors, and combinations thereof.

In some embodiments, antimetabolite agents include capecitabine, gemcitabine, and fluorouracil (5-FU).

In some embodiments, taxanes include paclitaxel, Abraxane® (paclitaxel protein-bound particles for injectable suspension), and Taxotere® (docetaxel).

In some embodiments, platinum analogs include oxaliplatin, cisplatin, and carboplatin.

In some embodiments, topoisomerase 1 inhibitors include irinotecan and topotecan.

In some embodiments, anthracyclines include doxorubicin or liposomal formulations of doxorubicin.

In some embodiments, the chemotherapeutic is FOLFIRINOX (5-FU, lecovorin, irinotecan and oxaliplatin). In some embodiments, the chemotherapeutic agent is gemcitabine and Abraxane® (paclitaxel protein-bound particles for injectable suspension).

In some embodiments, one or more JAK inhibitors of the invention can be used in combination with a chemotherapeutic in the treatment of cancer, such as multiple myeloma, and may improve the treatment response as compared to the response to the chemotherapeutic agent alone, without exacerbation of its toxic effects. Examples of additional pharmaceutical agents used in the treatment of multiple myeloma, for example, can include, without limitation, melphalan, melphalan plus prednisone [MP], doxorubicin, dexamethasone, and Velcade (bortezomib). Further additional agents used in the treatment of multiple myeloma include Bcr-Abl, Flt-3, RAF and FAK kinase inhibitors. Additive or synergistic effects are desirable outcomes of combining a JAK inhibitor of the present invention with an additional agent. Furthermore, resistance of multiple myeloma cells to agents such as dexamethasone may be reversible upon treatment with a JAK inhibitor of the present invention. The agents can be combined with the present compounds in a single or continuous dosage form, or the agents can be administered simultaneously or sequentially as separate dosage forms.

In some embodiments, a corticosteroid such as dexamethasone is administered to a patient in combination with at least one JAK inhibitor where the dexamethasone is administered intermittently as opposed to continuously.

In some further embodiments, combinations of one or more JAK inhibitors of the invention with other therapeutic agents can be administered to a patient prior to, during, and/or after a bone marrow transplant or stem cell transplant.

In some embodiments, the additional therapeutic agent is fluocinolone acetonide (Retisert®), or rimexolone (AL-2178, Vexol, Alcon).

In some embodiments, the additional therapeutic agent is cyclosporine (Restasis®).

In some embodiments, the additional therapeutic agent is a corticosteroid. In some embodiments, the corticosteroid is triamcinolone, dexamethasone, fluocinolone, cortisone, prednisolone, or flumetholone.

In some embodiments, the additional therapeutic agent is selected from Dehydrex™ (Holies Labs), Civamide (Opko), sodium hyaluronate (Vismed, Lantibio/TRB Chemedia), cyclosporine (ST-603, Sirion Therapeutics), ARG101(T) (testosterone, Argentis), AGR1012(P) (Argentis), ecabet sodium (Senju-Ista), gefarnate (Santen), 15-(s)-hydroxyeicosatetraenoic acid (15(S)-HETE), cevilemine, doxycycline (ALTY-0501, Alacrity), minocycline, iDestrin™ (NP50301, Nascent Pharmaceuticals), cyclosporine A (Nova22007, Novagali), oxytetracycline (Duramycin, MOLI1901, Lantibio), CF101 (2S,3S,4R,5R)-3,4-dihydroxy-5-[6-[(3-iodophenyl)methylamino]purin-9-yl]-N-methyl-oxolane-2-carbamyl, Can-Fite Biopharma), voclosporin (LX212 or LX214, Lux Biosciences), ARG103 (Agentis), RX-10045 (synthetic resolvin analog, Resolvyx), DYN15 (Dyanmis Therapeutics), rivoglitazone (DE011, Daiichi Sanko), TB4 (RegeneRx), OPH-01 (Ophtalmis Monaco), PCS101 (Pericor Science), REV1-31 (Evolutec), Lacritin (Senju), rebamipide (Otsuka-Novartis), OT-551 (Othera), PAI-2 (University of Pennsylvania and Temple University), pilocarpine, tacrolimus, pimecrolimus (AMS981, Novartis), loteprednol etabonate, rituximab, diquafosol tetrasodium (INS365, Inspire), KLS-0611 (Kissei Pharmaceuticals), dehydroepiandrosterone, anakinra, efalizumab, mycophenolate sodium, etanercept (Embrel®), hydroxychloroquine, NGX267 (TorreyPines Therapeutics), actemra, gemcitabine, oxaliplatin, L-asparaginase, or thalidomide.

In some embodiments, the additional therapeutic agent is an anti-angiogenic agent, cholinergic agonist, TRP-1 receptor modulator, a calcium channel blocker, a mucin secretagogue, MUC1 stimulant, a calcineurin inhibitor, a corticosteroid, a P2Y2 receptor agonist, a muscarinic receptor agonist, an mTOR inhibitor, another JAK inhibitor, Bcr-Abl kinase inhibitor, Flt-3 kinase inhibitor, RAF kinase inhibitor, and FAK kinase inhibitor such as, for example, those described in WO 2006/056399, which is incorporated herein by reference in its entirety. In some embodiments, the additional therapeutic agent is a tetracycline derivative (e.g., minocycline or doxycline). In some embodiments, the additional therapeutic agent binds to FKBP12.

In some embodiments, the additional therapeutic agent is an alkylating agent or DNA cross-linking agent; an anti-metabolite/demethylating agent (e.g., 5-flurouracil, capecitabine or azacitidine); an anti-hormone therapy (e.g., hormone receptor antagonists, SERMs, or aromotase inhibitor); a mitotic inhibitor (e.g. vincristine or paclitaxel); an topoisomerase (I or II) inhibitor (e.g. mitoxantrone and irinotecan); an apoptotic inducers (e.g. ABT-737); a nucleic acid therapy (e.g. antisense or RNAi); nuclear receptor ligands (e.g., agonists and/or antagonists: all-trans retinoic acid or bexarotene); epigenetic targeting agents such as histone deacetylase inhibitors (e.g. vorinostat), hypomethylating agents (e.g. decitabine); regulators of protein stability such as Hsp90 inhibitors, ubiquitin and/or ubiquitin like conjugating or deconjugating molecules; or an EGFR inhibitor (erlotinib).

In some embodiments, the additional therapeutic agent(s) are demulcent eye drops (also known as “artificial tears”), which include, but are not limited to, compositions containing polyvinylalcohol, hydroxypropyl methylcellulose, glycerin, polyethylene glycol (e.g. PEG400), or carboxymethyl cellulose. Artificial tears can help in the treatment of dry eye by compensating for reduced moistening and lubricating capacity of the tear film. In some embodiments, the additional therapeutic agent is a mucolytic drug, such as N-acetyl-cysteine, which can interact with the mucoproteins and, therefore, to decrease the viscosity of the tear film.

In some embodiments, the additional therapeutic agent includes an antibiotic, antiviral, antifungal, anesthetic, anti-inflammatory agents including steroidal and non-steroidal anti-inflammatories, and anti-allergic agents. Examples of suitable medicaments include aminoglycosides such as amikacin, gentamycin, tobramycin, streptomycin, netilmycin, and kanamycin; fluoroquinolones such as ciprofloxacin, norfloxacin, ofloxacin, trovafloxacin, lomefloxacin, levofloxacin, and enoxacin; naphthyridine; sulfonamides; polymyxin; chloramphenicol; neomycin; paramomycin; colistimethate; bacitracin; vancomycin; tetracyclines; rifampin and its derivatives (“rifampins”); cycloserine; beta-lactams; cephalosporins; amphotericins; fluconazole; flucytosine; natamycin; miconazole; ketoconazole; corticosteroids; diclofenac; flurbiprofen; ketorolac; suprofen; cromolyn; lodoxamide; levocabastin; naphazoline; antazoline; pheniramine; or azalide antibiotic.

Pharmaceutical Formulations and Dosage Forms

When employed as pharmaceuticals, the compounds of the invention can be administered in the form of pharmaceutical compositions. These compositions can be prepared in a manner well known in the pharmaceutical art, and can be administered by a variety of routes, depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including transdermal, epidermal, ophthalmic and to mucous membranes including intranasal, vaginal and rectal delivery), pulmonary (e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal or intranasal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal intramuscular or injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Parenteral administration can be in the form of a single bolus dose, or may be, for example, by a continuous perfusion pump. Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.

This invention also includes pharmaceutical compositions which contain, as the active ingredient, the compound of the invention or a pharmaceutically acceptable salt thereof, in combination with one or more pharmaceutically acceptable carriers (excipients). In some embodiments, the composition is suitable for topical administration. In making the compositions of the invention, the active ingredient is typically mixed with an excipient, diluted by an excipient or enclosed within such a carrier in the form of, for example, a capsule, sachet, paper, or other container. When the excipient serves as a diluent, it can be a solid, semi-solid, or liquid material, which acts as a vehicle, carrier or medium for the active ingredient. Thus, the compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, suppositories, sterile injectable solutions, and sterile packaged powders.

In preparing a formulation, the active compound can be milled to provide the appropriate particle size prior to combining with the other ingredients. If the active compound is substantially insoluble, it can be milled to a particle size of less than 200 mesh. If the active compound is substantially water soluble, the particle size can be adjusted by milling to provide a substantially uniform distribution in the formulation, e.g. about 40 mesh.

The compounds of the invention may be milled using known milling procedures such as wet milling to obtain a particle size appropriate for tablet formation and for other formulation types. Finely divided (nanoparticulate) preparations of the compounds of the invention can be prepared by processes known in the art, e.g., see International App. No. WO 2002/000196.

Some examples of suitable excipients include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, and methyl cellulose. The formulations can additionally include: lubricating agents such as talc, magnesium stearate, and mineral oil; wetting agents; emulsifying and suspending agents; preserving agents such as methyl- and propylhydroxy-benzoates; sweetening agents; and flavoring agents. The compositions of the invention can be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the patient by employing procedures known in the art.

In some embodiments, the pharmaceutical composition comprises silicified microcrystalline cellulose (SMCC) and at least one compound described herein, or a pharmaceutically acceptable salt thereof. In some embodiments, the silicified microcrystalline cellulose comprises about 98% microcrystalline cellulose and about 2% silicon dioxide w/w.

In some embodiments, the composition is a sustained release composition comprising at least one compound described herein, or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable carrier. In some embodiments, the composition comprises at least one compound described herein, or a pharmaceutically acceptable salt thereof, and at least one component selected from microcrystalline cellulose, lactose monohydrate, hydroxypropyl methylcellulose, and polyethylene oxide. In some embodiments, the composition comprises at least one compound described herein, or a pharmaceutically acceptable salt thereof, and microcrystalline cellulose, lactose monohydrate, and hydroxypropyl methylcellulose. In some embodiments, the composition comprises at least one compound described herein, or a pharmaceutically acceptable salt thereof, and microcrystalline cellulose, lactose monohydrate, and polyethylene oxide. In some embodiments, the composition further comprises magnesium stearate or silicon dioxide. In some embodiments, the microcrystalline cellulose is Avicel PH102™. In some embodiments, the lactose monohydrate is Fast-flo 316™. In some embodiments, the hydroxypropyl methylcellulose is hydroxypropyl methylcellulose 2208 K4M (e.g., Methocel K4 M Premier™) and/or hydroxypropyl methylcellulose 2208 K100LV (e.g., Methocel K00LV™). In some embodiments, the polyethylene oxide is polyethylene oxide WSR 1105 (e.g., Polyox WSR 1105™).

In some embodiments, a wet granulation process is used to produce the composition. In some embodiments, a dry granulation process is used to produce the composition.

The compositions can be formulated in a unit dosage form, each dosage containing from about 5 to about 1,000 mg (1 g), more usually about 100 mg to about 500 mg, of the active ingredient. In some embodiments, each dosage contains about 10 mg of the active ingredient. In some embodiments, each dosage contains about 50 mg of the active ingredient. In some embodiments, each dosage contains about 25 mg of the active ingredient. The term “unit dosage forms” refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient.

In some embodiments, the compositions of the invention contain from about 5 mg to about 50 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 5 mg to about 10 mg, about 10 mg to about 15 mg, about 15 mg to about 20 mg, about 20 mg to about 25 mg, about 25 mg to about 30 mg, about 30 mg to about 35 mg, about 35 mg to about 40 mg, about 40 mg to about 45 mg, or about 45 mg to about 50 mg of the active ingredient.

In some embodiments, the compositions of the invention contain from about 50 mg to about 500 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 50 mg to about 100 mg, about 100 mg to about 150 mg, about 150 mg to about 200 mg, about 200 mg to about 250 mg, about 250 mg to about 300 mg, about 350 mg to about 400 mg, or about 450 mg to about 500 mg of the active ingredient.

In some embodiments, the compositions of the invention contain from about 500 mg to about 1,000 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 500 mg to about 550 mg, about 550 mg to about 600 mg, about 600 mg to about 650 mg, about 650 mg to about 700 mg, about 700 mg to about 750 mg, about 750 mg to about 800 mg, about 800 mg to about 850 mg, about 850 mg to about 900 mg, about 900 mg to about 950 mg, or about 950 mg to about 1,000 mg of the active ingredient.

The active compound may be effective over a wide dosage range and is generally administered in a pharmaceutically effective amount. It will be understood, however, that the amount of the compound actually administered will usually be determined by a physician, according to the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.

For preparing solid compositions such as tablets, the principal active ingredient is mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound of the present invention. When referring to these preformulation compositions as homogeneous, the active ingredient is typically dispersed evenly throughout the composition so that the composition can be readily subdivided into equally effective unit dosage forms such as tablets, pills and capsules. This solid preformulation is then subdivided into unit dosage forms of the type described above containing from, for example, about 0.1 to about 1000 mg of the active ingredient of the present invention.

The tablets or pills of the present invention can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action. For example, the tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release. A variety of materials can be used for such enteric layers or coatings, such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac, cetyl alcohol, and cellulose acetate.

The liquid forms in which the compounds and compositions of the present invention can be incorporated for administration orally or by injection include aqueous solutions, suitably flavored syrups, aqueous or oil suspensions, and flavored emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil, or peanut oil, as well as elixirs and similar pharmaceutical vehicles.

Compositions for inhalation or insufflation include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders. The liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described supra. In some embodiments, the compositions are administered by the oral or nasal respiratory route for local or systemic effect. Compositions in can be nebulized by use of inert gases. Nebulized solutions may be breathed directly from the nebulizing device or the nebulizing device can be attached to a face masks tent, or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions can be administered orally or nasally from devices which deliver the formulation in an appropriate manner.

Topical formulations can contain one or more conventional carriers. In some embodiments, ointments can contain water and one or more hydrophobic carriers selected from, for example, liquid paraffin, polyoxyethylene alkyl ether, propylene glycol, white Vaseline, and the like. Carrier compositions of creams can be based on water in combination with glycerol and one or more other components, e.g. glycerinemonostearate, PEG-glycerinemonostearate and cetylstearyl alcohol. Gels can be formulated using isopropyl alcohol and water, suitably in combination with other components such as, for example, glycerol, hydroxyethyl cellulose, and the like. In some embodiments, topical formulations contain at least about 0.1, at least about 0.25, at least about 0.5, at least about 1, at least about 2, or at least about 5 wt % of the compound of the invention. The topical formulations can be suitably packaged in tubes of, for example, 100 g which are optionally associated with instructions for the treatment of the select indication, e.g., psoriasis or other skin condition.

The amount of compound or composition administered to a patient will vary depending upon what is being administered, the purpose of the administration, such as prophylaxis or therapy, the state of the patient, the manner of administration, and the like. In therapeutic applications, compositions can be administered to a patient already suffering from a disease in an amount sufficient to cure or at least partially arrest the symptoms of the disease and its complications. Effective doses will depend on the disease condition being treated as well as by the judgment of the attending clinician depending upon factors such as the severity of the disease, the age, weight and general condition of the patient, and the like.

The compositions administered to a patient can be in the form of pharmaceutical compositions described above. These compositions can be sterilized by conventional sterilization techniques, or may be sterile filtered. Aqueous solutions can be packaged for use as is, or lyophilized, the lyophilized preparation being combined with a sterile aqueous carrier prior to administration. The pH of the compound preparations typically will be between 3 and 11, more preferably from 5 to 9 and most preferably from 7 to 8. It will be understood that use of certain of the foregoing excipients, carriers, or stabilizers will result in the formation of pharmaceutical salts.

The therapeutic dosage of a compound of the present invention can vary according to, for example, the particular use for which the treatment is made, the manner of administration of the compound, the health and condition of the patient, and the judgment of the prescribing physician. The proportion or concentration of a compound of the invention in a pharmaceutical composition can vary depending upon a number of factors including dosage, chemical characteristics (e.g., hydrophobicity), and the route of administration. For example, the compounds of the invention can be provided in an aqueous physiological buffer solution containing about 0.1 to about 10% w/v of the compound for parenteral administration. Some typical dose ranges are from about 1 μg/kg to about 1 g/kg of body weight per day. In some embodiments, the dose range is from about 0.01 mg/kg to about 100 mg/kg of body weight per day. The dosage is likely to depend on such variables as the type and extent of progression of the disease or disorder, the overall health status of the particular patient, the relative biological efficacy of the compound selected, formulation of the excipient, and its route of administration. Effective doses can be extrapolated from dose-response curves derived from in vitro or animal model test systems.

The compositions of the invention can further include one or more additional pharmaceutical agents such as a chemotherapeutic, steroid, anti-inflammatory compound, or immunosuppressant, examples of which are listed hereinabove.

In some embodiments, the compound, or pharmaceutically acceptable salt thereof, is administered as an ophthalmic composition. Accordingly, in some embodiments, the methods comprise administration of the compound, or pharmaceutically acceptable salt thereof, and an ophthalmically acceptable carrier. In some embodiments, the ophthalmic composition is a liquid composition, semi-solid composition, insert, film, microparticles or nanoparticles.

In some embodiments, the ophthalmic composition is a liquid composition. In some embodiments, the ophthalmic composition is a semi-solid composition. In some embodiments, the ophthalmic composition is a topical composition. The topical compositions include, but are not limited to liquid and semi-solid compositions. In some embodiments, the ophthalmic composition is a topical composition. In some embodiments, the topical composition comprises aqueous solution, an aqueous suspension, an ointment or a gel. In some embodiments, the ophthalmic composition is topically applied to the front of the eye, under the upper eyelid, on the lower eyelid and in the cul-de-sac. In some embodiments, the ophthalmic composition is sterilized. The sterilization can be accomplished by known techniques like sterilizing filtration of the solution or by heating of the solution in the ampoule ready for use. The ophthalmic compositions of the invention can further contain pharmaceutical excipients suitable for the preparation of ophthalmic formulations. Examples of such excipients are preserving agents, buffering agents, chelating agents, antioxidant agents and salts for regulating the osmotic pressure.

As used herein, the term “ophthalmically acceptable carrier” refers to any material that can contain and release the compound, or pharmaceutically acceptable salt thereof, and that is compatible with the eye. In some embodiments, the ophthalmically acceptable carrier is water or an aqueous solution or suspension, but also includes oils such as those used to make ointments and polymer matrices such as used in ocular inserts. In some embodiments, the composition may be an aqueous suspension comprising the compound, or pharmaceutically acceptable salt thereof. Liquid ophthalmic compositions, including both ointments and suspensions, may have a viscosity that is suited for the selected route of administration. In some embodiments, the ophthalmic composition has a viscosity in the range of from about 1,000 to about 30,000 centipoise.

In some embodiments, the ophthalmic compositions may further comprise one or more of surfactants, adjuvants, buffers, antioxidants, tonicity adjusters, preservatives (e.g., EDTA, BAK (benzalkonium chloride), sodium chlorite, sodium perborate, polyquaterium-1), thickeners or viscosity modifiers (e.g., carboxymethyl cellulose, hydroxymethyl cellulose, polyvinyl alcohol, polyethylene glycol, glycol 400, propylene glycol hydroxymethyl cellulose, hydroxpropyl-guar, hyaluronic acid, and hydroxypropyl cellulose) and the like. Additives in the formulation may include, but are not limited to, sodium chloride, sodium bicarbonate, sorbic acid, methyl paraben, propyl paraben, chlorhexidine, castor oil, and sodium perborate.

Aqueous ophthalmic compositions (solutions or suspensions) generally do not contain physiologically or ophthalmically harmful constituents. In some embodiments, purified or deionized water is used in the composition. The pH may be adjusted by adding any physiologically and ophthalmically acceptable pH adjusting acids, bases or buffers to within the range of about 5.0 to 8.5. Ophthalmically acceptable examples of acids include acetic, boric, citric, lactic, phosphoric, hydrochloric, and the like, and examples of bases include sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate, tromethamine, trishydroxymethylamino-methane, and the like. Salts and buffers include citrate/dextrose, sodium bicarbonate, ammonium chloride and mixtures of the aforementioned acids and bases.

In some embodiments, the methods involve forming or supplying a depot of the therapeutic agent in contact with the external surface of the eye. A depot refers to a source of therapeutic agent that is not rapidly removed by tears or other eye clearance mechanisms. This allows for continued, sustained high concentrations of therapeutic agent to be present in the fluid on the external surface of the eye by a single application. Without wishing to be bound by any theory, it is believed that absorption and penetration may be dependent on both the dissolved drug concentration and the contact duration of the external tissue with the drug containing fluid. As the drug is removed by clearance of the ocular fluid and/or absorption into the eye tissue, more drug is provided, e.g. dissolved, into the replenished ocular fluid from the depot. Accordingly, the use of a depot may more easily facilitate loading of the ocular tissue for more insoluble therapeutic agents. In some embodiments, the depot can remain for up to eight hours or more. In some embodiments, the ophthalmic depot forms includes, but is not limited to, aqueous polymeric suspensions, ointments, and solid inserts.

In some embodiments, the ophthalmic composition is an ointment or gel. In some embodiment, the ophthalmic composition is an oil-based delivery vehicle. In some embodiments, the composition comprises a petroleum or lanolin base to which is added the active ingredient, usually as 0.1 to 2%, and excipients. Common bases may include, but are not limited to, mineral oil, petrolatum and combinations thereof. In some embodiments, the ointment is applied as a ribbon onto the lower eyelid.

In some embodiment, the ophthalmic composition is an ophthalmic insert. In some embodiments, the ophthalmic insert is biologically inert, soft, bio-erodible, viscoelastic, stable to sterilization after exposure to therapeutic agents, resistant to infections from air borne bacteria, bio-erodible, biocompatible, and/or viscoelastic. In some embodiments, the insert comprises an ophthalmically acceptable matrix, e.g., a polymer matrix. The matrix is typically a polymer and the therapeutic agent is generally dispersed therein or bonded to the polymer matrix. In some embodiments, the therapeutic agent may be slowly released from the matrix through dissolution or hydrolysis of the covalent bond. In some embodiments, the polymer is bioerodible (soluble) and the dissolution rate thereof can control the release rate of the therapeutic agent dispersed therein. In another form, the polymer matrix is a biodegradable polymer that breaks down such as by hydrolysis to thereby release the therapeutic agent bonded thereto or dispersed therein. In further embodiments, the matrix and therapeutic agent can be surrounded with an additional polymeric coating to further control release. In some embodiments, the insert comprises a biodegradable polymer such as polycaprolactone (PCL), an ethylene/vinyl acetate copolymer (EVA), polyalkyl cyanoacrylate, polyurethane, a nylon, or poly (dl-lactide-co-glycolide) (PLGA), or a copolymer of any of these. In some embodiments, the therapeutic agent is dispersed into the matrix material or dispersed amongst the monomer composition used to make the matrix material prior to polymerization. In some embodiments, the amount of therapeutic agent is from about 0.1 to about 50%, or from about 2 to about 20%. In further embodiments, the biodegradable or bioerodible polymer matrix is used so that the spent insert does not have to be removed. As the biodegradable or bioerodible polymer is degraded or dissolved, the therapeutic agent is released.

In further embodiments, the ophthalmic insert comprises a polymer, including, but are not limited to, those described in Wagh, et al., “Polymers used in ocular dosage form and drug delivery systems”, Asian J. Pharm., pages 12-17 (January 2008), which is incorporated herein by reference in its entirety. In some embodiments, the insert comprises a polymer selected from polyvinylpyrrolidone (PVP), an acrylate or methacrylate polymer or copolymer (e.g., Eudragit® family of polymers from Rohm or Degussa), hydroxymethyl cellulose, polyacrylic acid, poly(amidoamine) dendrimers, poly(dimethyl siloxane), polyethylene oxide, poly(lactide-co-glycolide), poly(2-hydroxyethylmethacrylate), poly(vinyl alcohol), or poly(propylene fumarate). In some embodiments, the insert comprises Gelfoam® R. In some embodiments, the insert is a polyacrylic acid of 450 kDa-cysteine conjugate.

In some embodiments, the ophthalmic composition is a ophthalmic film. Polymers suitable for such films include, but are not limited to, those described in Wagh, et al. (ibid). In some embodiments, the film is a soft-contact lens, such as ones made from copolymers of N,N-diethylacrylamide and methacrylic acid crosslinked with ethyleneglycol dimethacrylate.

In some embodiments, the ophthalmic composition comprises microspheres or nanoparticles. In some embodiment, the microspheres comprise gelatin. In some embodiments, the microspheres are injected to the posterior segment of the eye, in the choroidal space, in the sclera, intravitreally or sub-retinally. In some embodiments, the microspheres or nanoparticles comprises a polymer including, but not limited to, those described in Wagh, et al. (ibid), which is incorporated herein by reference in its entirety. In some embodiments, the polymer is chitosan, a polycarboxylic acid such as polyacrylic acid, albumin particles, hyaluronic acid esters, polyitaconic acid, poly(butyl)cyanoacrylate, polycaprolactone, poly(isobutyl)caprolactone, poly(lactic acid-co-glycolic acid), or poly(lactic acid). In some embodiments, the microspheres or nanoparticles comprise solid lipid particles.

In some embodiments, the ophthalmic composition comprises an ion-exchange resin. In some embodiments, the ion-exchange resin is an inorganic zeolite or synthetic organic resin. In some embodiments, the ion-exchange resin includes, but is not limited to, those described in Wagh, et al. (ibid), which is incorporated herein by reference in its entirety. In some embodiments, the ion-exchange resin is a partially neutralized polyacrylic acid.

In some embodiments, the ophthalmic composition is an aqueous polymeric suspension. In some embodiments, the therapeutic agent or a polymeric suspending agent is suspended in an aqueous medium. In some embodiments, the aqueous polymeric suspensions may be formulated so that they retain the same or substantially the same viscosity in the eye that they had prior to administration to the eye. In some embodiments, they may be formulated so that there is increased gelation upon contact with tear fluid.

Labeled Compounds and Assay Methods

Another aspect of the present invention relates to labeled compounds of the invention (radio-labeled, fluorescent-labeled, etc.) that would be useful not only in imaging techniques but also in assays, both in vitro and in vivo, for localizing and quantitating JAK in tissue samples, including human, and for identifying JAK ligands by inhibition binding of a labeled compound. Accordingly, the present invention includes JAK assays that contain such labeled compounds.

The present invention further includes isotopically-labeled compounds of the invention. An “isotopically” or “radio-labeled” compound is a compound of the invention where one or more atoms are replaced or substituted by an atom having an atomic mass or mass number different from the atomic mass or mass number typically found in nature (i.e., naturally occurring). Suitable radionuclides that may be incorporated in compounds of the present invention include but are not limited to ³H (also written as T for tritium), ¹¹C, ¹³C, ¹⁴C, ¹³N, ¹⁵N, ¹⁵O, ¹⁷O, ¹⁸O, ¹⁸F, ³⁵S, ³⁶Cl, ⁸²Br, ⁷⁵Br, ⁷⁶Br, ⁷⁷Br, ¹²³I, ¹²⁴I, ¹²⁵I and ¹³¹I. The radionuclide that is incorporated in the instant radio-labeled compounds will depend on the specific application of that radio-labeled compound. For example, for in vitro JAK labeling and competition assays, compounds that incorporate ³H, ¹⁴C, ⁸²Br, ¹²⁵I, ¹³¹I, ³⁵S or will generally be most useful. For radio-imaging applications ¹¹C, ¹⁸F, ¹²⁵I, ¹²³I, ¹²⁴I, ¹³¹I, ⁷⁵Br, ⁷⁶Br or ⁷⁷Br will generally be most useful.

It is to be understood that a “radio-labeled” or “labeled compound” is a compound that has incorporated at least one radionuclide. In some embodiments the radionuclide is selected from the group consisting of ³H, ¹⁴C, ¹²⁵I, ³⁵S and ⁸²Br. In some embodiments, the compound incorporates 1, 2, or 3 deuterium atoms.

The present invention can further include synthetic methods for incorporating radio-isotopes into compounds of the invention. Synthetic methods for incorporating radio-isotopes into organic compounds are well known in the art, and an ordinary skill in the art will readily recognize the methods applicable for the compounds of invention.

A labeled compound of the invention can be used in a screening assay to identify/evaluate compounds. For example, a newly synthesized or identified compound (i.e., test compound) which is labeled can be evaluated for its ability to bind a JAK by monitoring its concentration variation when contacting with the JAK, through tracking of the labeling. For example, a test compound (labeled) can be evaluated for its ability to reduce binding of another compound which is known to bind to a JAK (i.e., standard compound). Accordingly, the ability of a test compound to compete with the standard compound for binding to the JAK directly correlates to its binding affinity. Conversely, in some other screening assays, the standard compound is labeled and test compounds are unlabeled. Accordingly, the concentration of the labeled standard compound is monitored in order to evaluate the competition between the standard compound and the test compound, and the relative binding affinity of the test compound is thus ascertained.

Kits

The present invention also includes pharmaceutical kits useful, for example, in the treatment or prevention of JAK-associated diseases or disorders, such as cancer, which include one or more containers containing a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention. Such kits can further include, if desired, one or more of various conventional pharmaceutical kit components, such as, for example, containers with one or more pharmaceutically acceptable carriers, additional containers, etc., as will be readily apparent to those skilled in the art. Instructions, either as inserts or as labels, indicating quantities of the components to be administered, guidelines for administration, and/or guidelines for mixing the components, can also be included in the kit.

Synthesis

The compound of Formula Ia can be synthesized according to the embodiments above and as further illustrated by Schemes I-III below. In Scheme I, the nucleophilic coupling of (i) and (ii) in the presence of an amine base (e.g., N,N-diisopropylethylamine) affords the isomeric mixture of compounds (iii-a) and (iii-b). Subsequent reduction of the nitro group under hydrogenation conditions (e.g., in the presence of hydrogen gas and a hydrogen catalyst (e.g. palladium on carbon)) affords the isomeric mixture of compounds (iv-a) and (iv-b). Coupling of (iv-a) and (iv-b) with (R)-(+)-lactamide in the presence of an alkyloxonium reagent (e.g., triethyloxonium tetrafluoroborate) and subsequent cyclization affords the a mixture of the fused-tricyclic compounds of Formula Ia and Formula Ib. Subsequent reaction under reverse racemization conditions (e.g. in the presence of a strong base (e.g. potassium tert-butoxide)) yields a single isomer of the compound of Formula Ia, 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, which may be optionally hydrated to form the monohydrate compound of Formula II.

In Scheme II, compounds of Formula VI can be produced by reaction of (i) in the presence of a reducing agent (e.g., lithium borohydride) affords the amine-protected diol (ii), which is asymmetrically protected in the presence of 2,2-dimethoxypropane and boron trifluoride diethyl etherate to form oxazolidine (iii). Reaction of the free alcohol (iii) under oxidizing conditions affords the aldehyde (iv), which is then reacted under modified Wittig-Horner conditions (e.g. in the presence of diethyl (cyanomethyl)phosphonate and a potassium tert-butoxide) to form a mixture of the cis- and trans-isomers (v). Deprotection of (v) in the presence of a strong acid (e.g., p-toluenesulfonic acid) afford compound (vi), which is cyclized in the presence of a strong base (e.g. sodium methoxide) to form the amine-protected pyran of compound (vii). Deprotection under standard conditions (e.g., in the presence of a strong acid) affords the amine salt (viii).

In Scheme III, compounds of Formula VI can be produced. Accordingly, asymmetric carbonyl reduction of carboxylic acid (i) affords the hydroxy-ester compound (ii), which is subsequently cyclized in the presence of a weak organic acid (e.g. acetic acid) to form amino-lactone (iii). Reaction of (iii) under modified Wittig conditions (e.g., in the presence of cyanomethyl (trimethyl)phosphonium chloride and potassium tert-butoxide, or alternatively in the presence of tributyl(cyanomethyl)phosphonium chloride and potassium tert-butoxide) afford the mixture of cis- and trans-isomers of (iv). Reduction of the alkene (iv) in the presence of a hydrogen gas and a hydrogenation catalyst (e.g., palladium on carbon) affords the mixture of R- and S-isomers of (v). Deprotection of the amine under standard conditions (e.g., in the presence of a strong acid) affords amine salt (vi).

Intermediate (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole can be prepared, for example, according to the process shown in Scheme IV. For example, reaction of (R)-2-hydroxypropanamide (i) with 2,2-dimethoxypropane (ii) in the presence of a boron-trihalogen etherate (e.g., BF₃OEt₂) affords (R)-2,2,5-trimethyloxazolidin-4-one (iii). Reaction of compound (iii) with a methylating agent (e.g., Me₃O⁺BF₄ ⁻) and subsequent reaction in the presence of a base (e.g., sodium carbonate) affords (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole (v).

A mixture of the compounds of Formulae Ia and Ib can also be prepared, for example, according to the process shown in Scheme V. (R)-2,2,5-trimethyloxazolidin-4-one (i) is first reacted with a methylating agent (e.g., Me₃O⁺BF₄ ⁻) to form (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole (ii), which is subsequently reacted with a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (iii) to afford a mixture of the compounds of Formulae Ia and Ib (iv).

A mixture of the compounds of Formulae Ia and Ib can also be prepared, for example, according to the process shown in Scheme VI. (R)-2-hydroxypropanamide (i) is first protected under standard alcohol protection conditions (e.g., reaction with acetyl chloride) to form (R)-1-amino-1-oxopropan-2-yl acetate (ii), which is then reacted with cyanuric chloride to form (R)-1-cyanoethyl acetate (iii). Subsequent reaction of (iii) with ethanol in the presence of an acid catalyst (e.g., hydrogen chloride) affords (R)-ethyl 2-hydroxypropanimidate (iv) which is then reacted with a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (v) to form a mixture of the compounds of Formulae Ia and Ib (vi).

EXAMPLES

The invention will be described in greater detail by way of specific examples. The following examples are offered for illustrative purposes, and are not intended to limit the invention in any manner. Those of skill in the art will readily recognize a variety of noncritical parameters which can be changed or modified to yield essentially the same results.

Open access prep. LC-MS purification of some of the compounds prepared was performed on Waters mass directed fractionation systems. The basic equipment setup, protocols, and control software for the operation of these systems have been described in detail in literature. See e.g. “Two-Pump At Column Dilution Configuration for Preparative LC-MS”, K. Blom, J Combi. Chem., 4, 295 (2002); “Optimizing Preparative LC-MS Configurations and Methods for Parallel Synthesis Purification”, K. Blom, R. Sparks, J. Doughty, G. Everlof, T. Hague, A. Combs, J. Combi. Chem., 5, 670 (2003); and “Preparative LC-MS Purification: Improved Compound Specific Method Optimization”, K. Blom, B. Glass, R. Sparks, A. Combs, J. Combi. Chem., 6, 874-883 (2004). The compounds separated were typically subjected to analytical liquid chromatography mass spectrometry (LCMS) for purity under the following conditions: Instrument; Agilent 1100 series, LC/MSD, Column: Waters Sunfire™ C₁₈ 5 μm, 2.1×5.0 mm, Buffers: mobile phase A: 0.025% TFA in water and mobile phase B: 0.025% TFA in acetonitrile; gradient 2% to 80% of B in 3 minutes with flow rate 1.5 mL/minute.

Some of the compounds prepared were analyzed using Differential Scanning calorimetry (DSC). Typical DSC conditions are as follows:

TA Instruments Differential Scanning calorimetry, Model Q200 with autosampler. Temperature range: 30-350° C.; Temperature ramp rate: 10° C./min; Tzero aluminum sample pan and lid; nitrogen gas flow at 50 mL/min.

Some of the compounds prepared were analyzed using Thermogravimetric Analysis (TGA). Typical TGA conditions are as follows:

TA Instrument Thermogravimetric Analyzer, Model Q500. Temperature range: 20° C. to 600° C.; Temperature ramp rate: 20° C./min; nitrogen purge flow: 40 mL/min; Balance purge flow: 60 mL/min; Sample purge flow; platinum sample pan.

PerkinElmer Thermogravimetric Analyzer, Model Pyris 1. Temperature range: 25° C. to 300° C.; Temperature ramp rate: 10° C./min; Nitrogen purge gas flow: 60 mL/min; TGA ceramic crucible sample holder.

Some of the compounds prepared were analyzed using X-Ray Powder Diffraction (XRPD). Typical XRPD conditions are as follows:

Bruker D2 PHASER X-Ray Powder Diffractometer instrument; X-ray radiation wavelength: 1.05406 Å CuKAI; X-ray power: 30 KV, 10 mA; Sample powder: dispersed on a zero-background sample holder; General measurement conditions: Start Angle—5 degree; Stop Angle—60 degree; Sampling—0.015 degree; Scan speed—2 degree/min.

Rigaku MiniFlex X-ray Powder Diffractometer; X-ray radiation is from Copper Cu at 1.054056 Å with K_(β) filter; X-ray power: 30 KV, 15 mA; Sample powder: dispersed on a zero-background sample holder. General measurement condition: Start Angle—3 degree; Stop Angle—45 degree; Sampling—0.02 degree; Scan speed—2 degree/min.

Some of the compounds prepared were analyzed using Dynamic Vapor Sorption (DVS). Typical DVS conditions are as follows:

SGA-100 Symmetric Vapor Sorption Analyzer from VTI Corporation. The moisture uptake profile was completed in four cycles in 10% relative humidity (RH) increments with the first adsorption from 25% to 95% RH, followed by desorption in 10% increments from 95% to 5% RH. The equilibration criteria were 0.0050 wt % in 5 minutes with a maximum equilibration time of 180 minutes; Data logging interval: 2.00 min or 0.0100 wt %. All adsorption and desorption were performed at room temperature (25° C.). No pre-drying step was applied.

Some of the compounds prepared were analyzed after treatment in a humidity chamber. Typical humidity chamber conditions are as follows:

Temperature: 40° C.; Relative humidity: 75%; Time: 5 days.

Temperature: 30° C.; Relative humidity: 90%; Time: 7 days.

Example 1. 2-((2R,5S)-5-Aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride and 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride (Procedure 1)

Step 1. (S)-tert-Butyl 1,5-dihydroxypentan-2-ylcarbamate

In a 5-necked, 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, a reflux condenser, an addition funnel, and a nitrogen inlet was placed lithium borohydride (29.9 g, 1.37 mol, 2.0 eq.) at room temperature. Tetrahydrofuran (THF, 1.12 L) was charged to the flask while maintaining the internal temperature at below 40° C. The resulting solution was then cooled to 0-5° C. before a solution of (S)-dimethyl 2-(tert-butoxycarbonylamino)pentanedioate (189 g, 0.687 mol) in THF (0.60 L) was added over a period greater than 50 minutes via the addition funnel. The resulting reaction mixture was gradually warmed to room temperature and stirred at room temperature for 17 h and then cooled to 15° C. Methanol (MeOH, 415 mL) was then added dropwise to the reaction mixture over 3 h to quench residual lithium borohydride. During addition of methanol, vigorous gas evolution was observed. The quenched reaction mixture was then concentrated under reduced pressure to remove most of the solvents and the residue was treated with ethyl acetate (EtOAc, 350 mL) and water (300 mL). The resulting suspension was stirred at room temperature for 15 minutes before being filtered through a sintered funnel. The two phases of the filtrate were separated and the aqueous phase was extracted with EtOAc (100 mL). The combined organic phases were washed with brine (150 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford crude (S)-tert-butyl 1,5-dihydroxypentan-2-ylcarbamate (135 g, 89.7%) as a white solid, which was used in the subsequent reaction without further purification. ¹H NMR (400 MHz, DMSO-d₆) δ 6.42 (d, J=8.5 Hz, 1H), 4.52 (t, J=5.5 Hz, 1H), 4.33 (t, J=5.1 Hz, 1H), 3.42-3.21 (m, 4H), 3.18 (dt, J=10.5, 6.1 Hz, 1H), 1.54-1.44 (m, 1H), 1.41-1.28 (m, 11H), 1.22-1.16 (m, 1H) ppm.

Step 2. (S)-tert-Butyl 4-(3-hydroxypropyl)-2,2-dimethyloxazolidine-3-carboxylate

In a 5-necked, 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 1,5-dihydroxypentan-2-ylcarbamate (105 g, 0.479 mol) and acetone (4.0 L) at room temperature. The solution was then treated with 2,2-dimethoxypropane (64.8 g, 0.622 mol, 1.3 eq.) and boron trifluoride diethyl etherate (BF₃-Et₂O, 6.1 mL, 0.048 mol, 0.10 eq.) sequentially at room temperature. The resulting reaction mixture was stirred at room temperature for 18 h before triethylamine (TEA, 40.0 mL, 0.287 mol, 0.60 eq.) was added. The resulting mixture was then concentrated under reduced pressure to remove most of the solvents and the residue was treated with EtOAc (1000 mL) and water (200 mL). The two phases were separated and the organic phase was washed with brine (200 mL), dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (SiO₂, gradient elution with 0 to 50% of ethyl acetate in hexanes) to afford (S)-tert-butyl 4-(3-hydroxypropyl)-2,2-dimethyloxazolidine-3-carboxylate (95.0 g, 76.5%) as a colorless oil. ¹H NMR (400 MHz, DMSO-d₆) δ 4.39 (t, J=5.1 Hz, 1H), 3.85 (dd, J=8.7, 5.7 Hz, 1H), 3.72 (s, 1H), 3.66 (dd, J=8.8, 1.3 Hz, 1H), 3.42-3.32 (m, 2H), 1.61-1.54 (m, 1H), 1.51-1.24 (m, 18H) ppm.

Step 3. (S)-tert-Butyl 2,2-dimethyl-4-(3-oxopropyl)oxazolidine-3-carboxylate

In a 5-necked 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 4-(3-hydroxypropyl)-2,2-dimethyloxazolidine-3-carboxylate (110.0 g, 0.424 mol) and dichloromethane (DCM, 1200 mL) at room temperature. The resulting solution was then treated with 2,2,6,6-tetramethyl-1-piperidinyloxy free radical (TEMPO, 6.6 g, 0.042 mol, 0.10 eq.) and tetra-n-butylammonium chloride (11.8 g, 0.042 mol, 0.10 eq.) at room temperature before an aqueous solution of sodium bicarbonate (174 g, 2.08 mol, 5.0 eq) and an aqueous solution of potassium carbonate (28.7 g, 0.208 mol, 0.50 eq) were sequentially added to the reaction mixture at room temperature. While the resulting mixture was stirred vigorously, N-chlorosuccinimide (69.1 g, 0.518 mol, 1.22 eq.) was added at room temperature. The resulting reaction mixture was then stirred at room temperature for an additional 3 h before being transferred to a separation funnel. The two phases were separated and the aqueous phase was extracted with DCM (250 mL). The combined organic layers were washed with brine (2×300 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and dried under vacuum to afford crude (S)-tert-butyl 2,2-dimethyl-4-(3-oxopropyl)oxazolidine-3-carboxylate (109.1 g, 100%) as a pale orange oil, which was used in the subsequent reaction without further purification. ¹H NMR (300 MHz, DMSO-d₆) δ 9.64 (s, 1H), 4.01-3.60 (m, 3H), 2.39 (dd, J=10.9, 4.0 Hz, 2H), 1.84-1.64 (m, 2H), 1.47-1.38 (m, 15H) ppm.

Step 4. (S)-tert-Butyl 4-(4-cyanobut-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate

In a 3-necked, 3-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, and an addition funnel under nitrogen atmosphere was placed potassium tert-butoxide (1 M solution in THF, 1000 mL, 1.00 mol, 1.11 eq.) and tetrahydrofuran (THF, 700 mL) at room temperature. The solution was cooled to 0-5° C. and diethyl cyanomethylphosphonate (177.2 g, 1.00 mol, 1.11 eq.) was added dropwise via the addition funnel while maintaining the internal temperature at below 10° C. The resulting reaction mixture was then stirred at room temperature for 2 h, and labeled as Solution A for the subsequent reaction. In a separate 5-necked, 12-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 2,2-dimethyl-4-(3-oxopropyl)oxazolidine-3-carboxylate (232.0 g, 0.901 mol) and THF (3500 mL) at room temperature. The resulting solution was cooled to 0-5° C., and was labeled as Solution B. Solution A was then added to Solution B dropwise while maintaining the internal temperature at below 5° C. The resulting reaction mixture was gradually warmed to room temperature and stirred at room temperature for 1 h. Water (500 mL) was charged to the reaction mixture and two phases were separated. The aqueous phase was then extracted with EtOAc (2×100 mL). The combined organic phases were washed with brine (2×100 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (SiO₂, gradient elution with 0 to 30% of ethyl acetate in hexanes) to provide (S)-tert-butyl 4-(4-cyanobut-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate (179.0 g, 70.8%) as a colorless oil. ¹H NMR (300 MHz, DMSO-d₆) δ 6.84 (dt, J=16.4, 6.8 Hz, 0.5H), 6.66 (dt, J=10.9, 7.7 Hz, 0.5H), 5.83-5.51 (m, 1H), 3.92-3.49 (m, 3H), 2.35-2.05 (m, 2H), 1.73-1.52 (m, 2H), 1.45-1.38 (m, 15H).

Step 5. (S)-tert-Butyl 6-cyano-1-hydroxyhex-5-en-2-ylcarbamate

In a 5-necked, 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 4-(4-cyanobut-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate (179.0 g, 0.638 mol) and methanol (2000 mL) at room temperature. The resulting colorless solution was cooled to 0-5° C. before being treated with catalytic amount of p-toluenesulfonic acid (PTSA, 12.1 g, 0.064 mol, 0.10 eq.). The resulting reaction mixture was gradually warmed to room temperature and stirred at room temperature for an additional 17 h. An aqueous solution of sodium bicarbonate (100 mL) was then added to the reaction mixture at room temperature and the resulting mixture was concentrated under reduced pressure to about 500 mL. The residue was then extracted with ethyl acetate (2×500 mL). The combined organic phases were washed with brine (2×100 mL), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and dried under vacuum to afford crude (S)-tert-butyl 6-cyano-1-hydroxyhex-5-en-2-ylcarbamate (144.2 g, 94%) as a light pink oil, which was used in the subsequent reaction without further purification. ¹H NMR (300 MHz, CDCl₃) δ 6.72 (dt, J=16.3, 6.9 Hz, 0.5H), 6.53 (dt, J=10.9, 7.6 Hz, 0.5H), 5.51-5.08 (m, 1H), 4.73 (s, 1H), 3.83-3.34 (m, 3H), 2.49 (dt, J=11.3, 5.9 Hz, 1H), 2.31 (q, J=7.0 Hz, 1H), 1.74-1.57 (m, 3H), 1.44 (s, 9H).

Step 6. (S)-tert-Butyl 6-(cyanomethyl)tetrahydro-2H-pyran-3-ylcarbamate (Mixture of Cis- and Trans-Isomers)

In a 5-necked, 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 6-cyano-1-hydroxyhex-5-en-2-ylcarbamate (173.0 g, 0.720 mol) and tetrahydrofuran (1700 mL) at room temperature. The solution was cooled to 0-5° C. before a solution of sodium methoxide (0.5 M solution in methanol, 21.30 mL, 0.011 mol, 0.015 eq) in THF (90 mL) was added dropwise via the addition funnel while maintaining the internal temperature at below 5° C. The resulting reaction mixture was stirred at below 5° C. for an additional 1 h before brine (500 mL) and tert-butyl methyl ether (TBME, 400 mL) were added to the reaction mixture sequentially. The two phases were separated and the aqueous phase was extracted with TBME (250 mL). The combined organic phases were washed with brine (250 mL), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and dried under vacuum to afford crude (S)-tert-butyl 6-(cyanomethyl)tetrahydro-2H-pyran-3-ylcarbamate (173.0 g, 100%) as a viscous solid. The crude product, obtained as a mixture of cis- and trans-isomers, was used in the subsequent reaction without further purification. ¹H NMR (400 MHz, CDCl₃) δ 5.13 (s, 0.5H), 4.25 (s, 0.5H), 4.10 (ddd, J=10.9, 4.7, 2.2 Hz, 0.5H), 3.89 (d, J=12.1 Hz, 0.5H), 3.72 (s, 0.5H), 3.66-3.57 (m, 1.5H), 3.56-3.49 (m, 0.5H), 3.03 (t, J=10.8 Hz, 0.5H), 2.54 (dd, J=6.0, 2.5 Hz, 2H), 2.19-2.08 (m, 0.5H), 2.00 (d, J=13.2 Hz, 0.5H), 1.87 (d, J=13.1 Hz, 0.5H), 1.65-1.62 (m, 2H), 1.44 (d, J=6.5 Hz, 9H), 1.38-1.24 (m, 0.5H).

Step 7. 2-((2R,5S)-5-Aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride and 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride (Mixture of Trans- and Cis-Isomers)

In a 5-necked, 5-L round bottom flask equipped with an overhead mechanical stirrer, a thermocouple, an addition funnel, and a nitrogen inlet was placed (S)-tert-butyl 6-(cyanomethyl)tetrahydro-2H-pyran-3-ylcarbamate (a mixture of cis- and trans-isomers, 173.0 g, 0.720 mol) and dichloromethane (1730 mL) at room temperature. The resulting solution was then treated with a solution of 4.0 M hydrogen chloride (HCl) in 1,4-dioxane (720 mL, 2.880 mol, 4.0 eq.) via the addition funnel. The resulting reaction mixture was stirred at room temperature for 2 h before tert-butyl methyl ether (TBME, 1000 mL) was added. The resulting suspension was stirred at room temperature for 30 minutes. The white solids formed were collected by filtration, washed with TBME (280 mL), and dried in a vacuum oven with nitrogen sweeping at 50° C. to afford 2-((2R,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride and 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride (114.0 g, 89.6%) as a mixture of trans- and cis-isomers. ¹H NMR (400 MHz, DMSO-d₆) δ 8.31 (s, 3H), 4.03 (ddd, J=10.8, 4.5, 2.2 Hz, 0.5H), 3.92 (d, J=12.6 Hz, 0.5H), 3.71-3.58 (m, 1H), 3.51 (ddp, J=8.8, 4.4, 2.1 Hz, 0.5H), 3.36 (s, 0.5H), 3.25 (s, 0.5H), 3.04 (s, 0.5H), 2.87-2.56 (m, 2H), 2.08 (d, J=12.7 Hz, 0.5H), 1.98-1.72 (m, 1.5H), 1.70-1.46 (m, 1.5H), 1.36 (qd, J=13.2, 3.9 Hz, 0.5H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 118.48 (118.33), 72.52 (72.07), 67.75 (67.56), 45.53 (44.36), 28.59 (24.33), 26.78 (24.06), 23.42 (23.14) ppm; LCMS calculated for C₇H₁₂N₂O: 140.2 (free amine), Found: 141 (M⁺+H); Salt ratio (HCl to the free amine): 1.00.

Example 2. 2-((2R,5S)-5-Aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride and 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride (Procedure 2)

Step 1. methyl (4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate

A solution of (2S)-2-[(tert-butoxycarbonyl)amino]-5-methoxy-5-oxopentanoic acid (40.00 g, 153.1 mmol) in tetrahydrofuran (600 mL) was treated with 4-methylmorpholine (17 g, 168.1 mmol, 1.1 eq.) at room temperature. The resulting mixture was cooled to 0° C. before being treated with ethyl chloroformate (18 g, 165.9 mmol, 1.08 eq.) dropwise. The resulting reaction mixture was stirred at 0° C. for an additional 20 minutes before being filtered through Celite. The Celite bed was washed with THF (50 mL) and the clear filtrate solution was cooled to 0° C. The cooled solution was then treated with solid NaBH₄ (3.00 g, 79.3 mmol, 0.52 eq.) followed by a solution of NaBH₄ (2.9 g, 76.1 mmol, 0.50 eq.) in diglyme (40 mL). The resulting reaction mixture was stirred at room temperature for 3 h before being treated with an aqueous 1.0 M HCl solution (100 mL). The mixture was then stirred at room temperature for 10 minutes. The inorganic solids were filtered off and rinsed with EtOAc (100 mL). Ethyl acetate (1100 mL) was then added into the filtrate and the combined filtrate solution was concentrated under reduced pressure to remove the solvents (1200 mL). The remaining mixture was then washed with saturated aqueous sodium bicarbonate (50 mL) and water (2×50 mL). The organic phase was then concentrated under reduced pressure to afford crude methyl (4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate (37.9 g), which was used in the subsequent reaction without further purification.

Step 2. (9-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate

A solution of crude methyl (4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate (37.9 g, 153.1 mmol) in toluene (600 mL) and acetic acid (200 mL) was heated to reflux for 60 minutes. The solvents were then removed by the azeotropic distillation at atmospheric pressure. During the azeotropic distillation, an additional amount of toluene (600 mL) was introduced and a total of 1200 mL of the mixed solvents was removed. The residual mixture was then cooled to room temperature over 3 h and stirred at room temperature for 2 h. The solids were collected by filtration, washed with n-heptane (100 mL), and dried under reduced pressure at below 40° C. to afford the desired tert-butyl [(3S)-6-oxotetrahydro-2H-pyran-3-yl]carbamate (25 g, 75% overall yield for two steps). ¹H NMR (400 MHz, CDCl₃) δ 4.39 (dd, J=11.5, 5.4 Hz, 1H), 4.18 (dd, J=11.4, 4 Hz, 1H), 4.00 (s, 1H), 2.69-2.54 (m, 2H), 2.22 (dq, J=13.2, 6.6 Hz, 1H), 1.86 (dq, J=14.6, 7.3 Hz, 1H), 1.43 (s, 9H); GCMS Calculated for C₁₀H₁₇NO₄: 215.25; Found: 215.1.

Step 3. tert-Butyl [(3S,6Z)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6E)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate

Method A.

A solution of cyanomethyl (trimethyl)phosphonium chloride (8.8 g, 58.06 mmol, 1.25 eq.) in N,N-dimethylacetamide (DMAC, 50 ml) was degassed and cooled to 0° C. The chilled solution was then treated with a solution of 1.0 M lithium hexamethyldisilazide in THF (LHMDS, 53.4 mL, 53.4 mmol, 1.15 eq.) at 0° C. The resulting mixture was stirred at 0° C. for 60 minutes before being treated with a solution of tert-butyl [(3S)-6-oxotetrahydro-2H-pyran-3-yl]carbamate (10 g, 46.46 mmol) in THF (40 mL) at 0° C. The reaction mixture was stirred at 0° C. for 2 h followed by stirring overnight at room temperature. The reaction mixture was then quenched with water (100 mL) and the two phases were separated. The aqueous phase was extracted with tert-butyl methyl ether (TBME, 2×150 mL). The combined organic phase was washed with water (2×150 mL) before being concentrated under reduced pressure to afford the crude desired product (11 g, 99%) as a mixture of tert-butyl [(3S,6Z)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6E)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate, which was used in the subsequent reaction without further purification and separation. Analytical samples of the individual isomers were obtained by silica gel column chromatography (SiO₂, gradient elution with 0-30% of t-Butyl methyl ether (MTBE) in heptane).

For (3S,6E)-isomer: ¹H NMR (400 MHz, CDCl₃) δ 4.82 (s, 1H), 4.67 (s, 1H). 4.12 (dd, 1H), 3.93 (m, 1H), 3.81 (dd, 1H), 2.79 (dt, 1H), 2.58 (m, 1H), 2.12 (dt, 1H), 1.69 (dt, 1H), 1.40 (s, 9H); GCMS Calculated for C₁₂H₁₈N₂O₃: 238.28; Found: 238.1.

For (3S,6Z)-isomer: ¹H NMR (400 MHz, CDCl₃) δ 4.81 (s, 1H), 4.48 (s, 1H), 4.19 (dt, 1H), 3.95 (m, 2H). 2.48 (m, 2H), 2.09 (m, 1H), 1.58 (m, 1H), 1.40 (s, 9H); GCMS Calculated for C₁₂H₁₈N₂O₃: 238.28; Found: 238.1.

Method B.

A mixture of tributyl(cyanomethyl)phosphonium chloride (593 g, 2.14 mol) in THF (5.9 L) was treated with solid potassium tert-butoxide (220 g, 1.97 mol) in portions at 0° C. over 5 minutes. The resulting mixture was gradually warmed to room temperature over 4 h. The resulting ylide solution was then treated with (S)-tert-butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate (184 g, 0.855 mol) as a solid at room temperature and the resulting reaction mixture was heated at 70° C. and stirred at 70° C. for 16 h. When NMR analysis indicated that the starting material was consumed, the reaction mixture was gradually cooled to room temperature. The resulting slurry was poured into a 50-L separation funnel containing saturated aqueous sodium bicarbonate (5 L) and ice (1000 g). Ethyl acetate (6 L) was added and the mixture was stirred for 10 minutes. The two layers were separated and the aqueous layer was extracted with EtOAc (3 L). The combined organic layers were washed with saturated aqueous sodium chloride (3×4 L), dried over sodium sulfate, and concentrated under reduced pressure. The resulting dark oil was dissolved in DCM (500 mL) and purified by column chromatography (SiO₂, gradient elution with 20-40% ethyl acetate in heptanes) to afford the desired product (177 g, 87% yield) as a mixture of tert-butyl [3S,6Z)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [3S,6E)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate, which was used in the subsequent reaction without further purification and separation. Analytical samples of the two isomers were obtained by silica gel column chromatography (SiO₂, gradient elution with 0-30% of t-butyl methyl ether (TBME) in heptane).

For (3S,6E)-isomer: ¹H NMR (400 MHz, CDCl₃) δ 4.82 (s, 1H), 4.67 (s, 1H). 4.12 (dd, 1H), 3.93 (m, 1H), 3.81 (dd, 1H), 2.79 (dt, 1H), 2.58 (m, 1H), 2.12 (dt, 1H), 1.69 (dt, 1H), 1.40 (s, 9H); GCMS Calculated for C₁₂H₁₈N₂O₃: 238.28; Found: 238.1.

For (3S,6Z)-isomer: ¹H NMR (400 MHz, CDCl₃) δ 4.81 (s, 1H), 4.48 (s, 1H), 4.19 (dt, 1H), 3.95 (m, 2H), 2.48 (m, 2H), 2.09 (m, 1H), 1.58 (m, 1H), 1.40 (s, 9H); GCMS Calculated for C₁₂H₁₈N₂O₃: 238.28; Found: 238.1.

Step 4. tert-Butyl [(3S,6S)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6R)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate

A mixture of tert-butyl [(3S,6Z)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6E)-6-(cyanomethylene)tetrahydro-2H-pyran-3-yl]carbamate (110 g, 0.462 mol) and palladium on carbon (10 wt % Pd—C, 50% wet, 14 g) in methanol (1.1 L) was hydrogenated at 20 psi until hydrogen uptake ceased (4 to 12 h). The reaction mixture was filtered through Celite (100 g) and the Celite bed was washed with methanol (500 mL). The combined filtrate was concentrated under reduced pressure to afford the crude reduction products as an off-white solid. The crude products were further dried by azeotropic distillation with toluene (2×500 mL) and n-heptane (2×500 mL) under reduced pressure to remove residual methanol and water to afford tert-butyl [(3S,6S)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6R)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate (111 g, nearly quantitative yield) as a mixture of diastereomers, which was used directly in the subsequent reaction without further purification and separation. ¹H NMR (300 MHz, CDCl₃, as a mixture of two diastereomers) δ 5.15 (br s, 1H), 4.29 (br s, 1H), 4.14-4.07 (m, 1H), 3.94-3.87 (m, 1H), 3.77-3.44 (m, 5H), 3.09-3.01 (m, 1H), 2.58-2.49 (m, 4H), 2.18-2.09 (m, 1H), 2.05-1.95 (m, 1H), 1.92-1.81 (m, 1H), 1.76-1.51 (m, 5H), 1.46 (s, 9H), 1.44 (s, 9H); GCMS calculated for C₁₂H₂₀N₂O₃: 240.30; Found: 240.1.

Step 5. 2-((2S,5S)-5-Aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride and 2-((2R,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile Hydrochloride

A solution of tert-butyl [(3S,6S)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate and tert-butyl [(3S,6R)-6-(cyanomethyl)tetrahydro-2H-pyran-3-yl]carbamate (240 g, 0.999 mol) in dichloromethane (2.44 L) was treated with a solution of 4 M HCl in 1,4-dioxane (1 L, 3.99 mol, 4.0 eq.) dropwise over 30 minutes while keeping the internal temperature at below 25° C. The resulting reaction mixture was stirred at room temperature for 3 h. When ¹H NMR analysis of the filtered sample indicated that the reaction was complete, tert-butyl methyl ether (TBME, 675 mL) was added to the reaction mixture and the resulting mixture was stirred at room temperature for 30 minutes. The white solids formed were collected by filtration under a blanket of nitrogen, washed with TBME (600 mL), and further dried in a vacuum oven under a blanket of nitrogen for 16 h to afford 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride and 2-((2R,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride (151.7 g, 86% yield) as a mixture of cis- and trans-isomers. ¹H NMR (400 MHz, DMSO-d₆) (a mixture of cis- and trans-isomers) δ 8.31 (s, 3H), 4.03 (ddd, J=10.8, 4.5, 2.2 Hz, 0.5H), 3.92 (d, J=12.6 Hz, 0.5H), 3.71-3.58 (m, 1H), 3.51 (ddp, J=8.8, 4.4, 2.1 Hz, 0.5H), 3.36 (s, 0.5H), 3.25 (s, 0.5H), 3.04 (s, 0.5H), 2.87-2.56 (m, 2H), 2.08 (d, J=12.7 Hz, 0.5H), 1.98-1.72 (m, 1.5H), 1.70-1.46 (m, 1.5H), 1.36 (qd, J=13.2, 3.9 Hz, 0.5H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 118.48 (118.33), 72.52 (72.07), 67.75 (67.56), 45.53 (44.36), 28.59 (24.33), 26.78 (24.06), 23.42 (23.14) ppm; LCMS Calculated for C₇H₁₂N₂O: 140.2 (free amine), Found: 141 (M⁺+H); salt ratio (HCl to the free amine): 1.00.

Example 3. 2-((2R,5S)-5-(6-Nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile

A mixture of 2-((2S,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride and 2-((2R,5S)-5-aminotetrahydro-2H-pyran-2-yl)acetonitrile hydrochloride (2464 g, 13.95 mol, 1.16 eq.), and 7-chloro-6-nitrothieno[3,2-b]pyridine (2581 g, 12.02 mol) in N,N-dimethylformamide (DMF, 12.3 L) was treated with diisopropylethylamine (DIPEA, 4897 g, 46.13 mol, 3.84 eq.) at room temperature. The resulting reaction mixture was heated to 65-75° C. for 2-6 h until HPLC showed the reaction was complete. Water (36.9 L) was added to the reaction mixture at above 55° C. to precipitate the crude desired product and the resulting mixture was gradually cooled to 15-30° C. and stirred at 15-30° C. for 1-2 h. The yellow solids were collected by filtration, washed with water (36.9 L) and n-heptane (30.8 L), and dried in a vacuum oven at 45-50° C. to constant weight to afford the crude desired product (3550 g, 92.8%) as a mixture of 2-((2R,5S)-5-(6-nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile, which was used in the subsequent reaction without further purification and separation. Analytical samples of the cis-isomer and trans-isomer were obtained by column chromatography separation (SiO₂, gradient elution with 0-50% of ethyl acetate in heptane).

For (2R,5S)-isomer: ¹H NMR (400 MHz, DMSO-d₆) δ 9.09 (s, 1H), 8.87 (d, J=9.1 Hz, 1H), 8.35 (d, J=5.5 Hz, 1H), 7.53 (d, J=5.5 Hz, 1H), 4.32 (ddq, J=14.4, 10.1, 4.3 Hz, 1H), 4.17 (ddd, J=10.9, 4.5, 2.2 Hz, 1H), 3.66 (ddd, J=9.2, 6.8, 4.5 Hz, 1H), 3.52 (t, J=10.6 Hz, 1H), 2.85 (dd, J=17.0, 4.4 Hz, 1H), 2.76 (dd, J=17.0, 6.8 Hz, 1H), 2.28-2.23 (m, 1H), 191-1.81 (m, 2H), 1.61-1.43 (m, 1H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 159.30, 147.11, 145.78, 136.17, 125.59, 125.47, 118.47, 116.54, 71.79, 70.18, 50.25, 29.95, 29.18, 23.14 ppm; C₁₄H₁₄N₄O₃S (MW 318.3), LCMS (EI) m/e 319 (M⁺+H).

For (2S,5S)-isomer ¹H NMR (400 MHz, DMSO-d₆) δ 9.69 (d, J=8.5 Hz, 1H), 9.14 (s, 1H), 8.37 (d, J=5.5 Hz, 1H), 7.54 (d, J=5.5 Hz, 1H), 4.49 (d, J=8.6 Hz, 1H), 4.03 (d, J=11.9 Hz, 1H), 3.89 (d, J=10.4 Hz, 1H), 3.75 (dd, J=7.1, 3.6 Hz, 1H), 2.84 (dd, J=17.1, 4.3 Hz, 1H), 2.71 (dd, J=17.1, 7.0 Hz, 1H), 2.07-2.04 (m, 2H), 1.75-1.40 (m, 2H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 159.15, 147.26, 145.49, 136.22, 125.56, 125.28, 118.16, 116.77, 72.53, 70.31, 47.99, 27.84, 25.08, 23.65 ppm; C₁₄H₁₄N₄O₃S (MW 318.3), LCMS (EI) m/e 319 (M⁺+H).

Example 4. 2-((2R,5S)-5-(6-Aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile

A solution of 2-((2R,5S)-5-(6-nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-nitrothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (2000 g, 6.28 mol) in 2,2,2-trifluoroethanol (8.1 L) was treated with palladium on carbon (10 wt % Pd—C, 50% wet, 200 g) at room temperature. The resulting reaction mixture was degassed and refilled with nitrogen gas three times followed by hydrogen gas, three times. The hydrogenation reaction was run at 20-35° C. with 50 psi of hydrogen pressure. When HPLC showed the reaction was complete, the pressure was reduced to atmospheric before being degassed and refilled with nitrogen three times. The mixture was then filtered through Celite (667 g) and the Celite bed was rinsed with methanol (8 L). The filtrate was then concentrated under reduced pressure at below 50° C. to afford the desired crude product (2242 g) as a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile. This mixture, obtained as foam which contained residual solvents was inseparable on a silica gel column, and was used in the subsequent reaction without further purification.

For (2R,5S)-isomer: ¹HNMR (400 MHz, DMSO-d₆) δ 7.93 (s, 1H), 7.55 (d, J=5.6 Hz, 1H), 7.20 (d, J=5.6 Hz, 1H), 4.91 (d, J=9.7 Hz, 1H), 4.82 (s, 2H), 4.06-3.77 (m, 2H), 3.55 (dtt, J=8.7, 4.5, 2.1 Hz, 1H), 3.24 (t, J=10.3 Hz, 1H), 2.92-2.62 (m, 2H), 2.20-1.97 (m, 1H), 1.88-1.70 (m, 1H), 1.66-1.51 (m, 1H), 1.50-1.37 (m, 1H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 150.28, 136.88, 134.86, 128.10, 124.86, 124.82, 118.55, 117.95, 72.14, 71.70, 49.30, 30.79, 29.74, 23.32 ppm; C₁₄H₁₆N₄OS (MW 288.3), LCMS (EI) m/e 289 (M⁺+H).

For (2S,5S)-isomer: ¹H NMR (400 MHz, DMSO-d₆) δ 8.01 (s, 1H), 7.59 (d, J=5.5 Hz, 1H), 7.22 (d, J=5.5 Hz, 1H), 5.09 (d, J=9.6 Hz, 1H), 4.76 (s, 2H), 3.99 (d, J=9.6 Hz, 1H), 3.87 (d, J=11.7 Hz, 1H), 3.75 (dd, J=11.7, 2.2 Hz, 1H), 3.66 (dddd, J=10.3, 7.2, 4.4, 2.6 Hz, 1H), 2.85-2.62 (m, 2H), 1.86-1.69 (m, 2H), 1.63 (qd, J=12.7, 12.2, 4.4 Hz, 1H), 1.52-1.44 (m, 1H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 150.81, 137.91, 135.84, 128.17, 125.36, 124.83, 118.71, 118.61, 72.37, 70.23, 46.81, 27.08, 24.94, 23.44 ppm; C₁₄H₁₆N₄OS (MW 288.3), LCMS (EI) m/e 289 (M⁺+H).

Example 5. 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile

In reactor A, a suspension of (R)-(+)-lactamide (2045 g, 22.96 mol, 3.0 eq.) in THF (10.1 L) was treated with Et₃O—BF₄ (4405 g, 22.96 mol, 3.0 eq.) at −10 to 0° C. The resulting mixture in reactor A was then stirred at below 10° C. until a clear solution was formed. In reactor B, a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (2207 g, 7.65 mol) in ethanol (66.2 L) was heated to reflux to provide a clear solution. The solution in reactor A was then gradually added to the mixture in reactor B while maintaining the mixture in reactor B at reflux. The resulting reaction mixture in reactor B was maintained at reflux until HPLC showed the reaction was complete. The reaction mixture in reactor B was then cooled to 10-30° C. before an aqueous solution of sodium bicarbonate (664 g, 7.4 L) was gradually added. During addition of aqueous sodium bicarbonate to adjust the pH to 8-9, the internal temperature was controlled at below 35° C. The resulting mixture was then stirred at room temperature for an additional 30 minutes before being filtered through Celite (1 kg). After the filtration, the Celite bed was rinsed with ethanol (5.0 L). The combined filtrate was concentrated under reduced pressure at below 60° C. and dichloromethane (17.7 L) was added to dissolve the residue. The resulting DCM solution was then treated with a 1 N aqueous HCl solution (19.0 L) to adjust the pH of the aqueous phase to 1. The mixture was then stirred for 30 minutes at room temperature. The two phases were separated and the DCM phase was discarded. The acidic aqueous phase was then washed with DCM (8.6 L). The two phases were separated and the DCM phase was discarded. The acidic aqueous phase was then treated with ethyl acetate (30.6 L) followed by solid sodium carbonate (540 g). The resulting mixture was stirred at room temperature until the aqueous phase reached a pH of 9-10. n-Heptane (60.0 L) was then added to the mixture, and the resulting mixture was stirred at room temperature for at least 1 h. The solids were collected by filtration and washed with water (8.6 L) and n-heptane (8.6 L) before being dissolved in a mixture of methanol and DCM. The resulting solution of MeOH and DCM was then passed through a silica gel bed and the silica gel bed was washed with a mixture of MeOH and DCM (1 to 9 by volume). The combined solution was concentrated under reduced pressure to afford a first crop of the desired product (1450 g), a mixture 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, as white foam. The two phases of the filtrate were then separated and the aqueous phase was extracted with DCM (2×25.0 L). The combined organic extracts were concentrated under reduced pressure and the residue was purified by silica gel column chromatography (SiO₂, gradient elution with 0.5% to 7.5% MeOH in DCM) to afford a second crop of the desired product (515 g; total 1965 g, 75%), also as a mixture 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, as white foam. The mixture of two diastereomers was inseparable by silica gel column chromatography, and was used in the subsequent reaction without further separation.

For (2R,5S)-isomer: ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

For (2S,5S)-isomer: ¹H NMR (400 MHz, CD₃CN) δ 8.93 (s, 1H), 7.80 (d, J=5.5 Hz, 1H), 7.63 (d, J=5.5 Hz, 1H), 5.38 (s, 1H), 5.00 (dq, J=9.4, 4.7 Hz, 1H), 4.43 (dd, J=11.8, 9.3 Hz, 1H), 4.26 (dd, J=8.6, 3.7 Hz, 1H), 4.16 (s, 1H), 4.03-3.89 (m, 1H), 3.17 (dd, J=17.1, 8.6 Hz, 1H), 2.87 (dd, J=17.2, 5.4 Hz, 1H), 2.57 (dtd, J=14.8, 10.8, 4.2 Hz, 1H), 2.20-1.99 (m, 2H), 1.88-1.82 (m, 1H), 1.73 (d, J=6.4 Hz, 3H) ppm; ¹³C NMR (101 MHz, CD₃CN) δ 158.04, 152.88, 142.12, 136.81, 136.46, 127.44, 127.14, 119.04, 116.97, 70.00, 64.83, 64.03, 54.55, 28.06, 25.73, 22.46, 21.94 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

Example 6. 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate (Crude Product)

A mixture of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (800 g, 2.34 mol) in 2-propanol (IPA, 16 L) was treated with a solution of 1.0 M potassium tert-butoxide in THF (234 mL, 0.234 mol, 0.10 eq.) at room temperature. The resulting reaction mixture was stirred at room temperature for 20 h. When HPLC showed the base-promoted racemization reaction was complete, the reaction mixture was treated with a 0.1 M aqueous HCl solution (approximately 2.4 L) to adjust the pH to 6-7. The mixture was then concentrated under reduced pressure at below 50° C. to partially remove IPA (approximately 9.6 L) and the residue was treated with water (10.5 L) at room temperature. The resulting mixture was then stirred at room temperature for 2 h. The solids were collected by filtration, washed with a mixture of IPA and water (2.4 L, 1 to 2 by volume), and dried under reduced pressure at below 50° C. to constant weight to provide crude 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate (657 g, 78%) as a white solid. ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H); water content by KF: 5.15%.

Example 7. 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (Anhydrous Crystalline Free Base)

A solution of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate (650 g, 1.80 mol) in methanol (7 L) was polish filtered before being concentrated at atmospheric pressure to remove methanol (5 L). The resulting concentrated solution was then treated with ethyl acetate (8.5 L) and the atmospheric distillation was continued to remove solvents (5.3 L). n-Heptane (7.8 L) was then gradually added to the residual mixture at 60-75° C. and the resulting mixture was gradually cooled down to room temperature and stirred at room temperature for at least 1.5 h. The solids were collected by filtration, washed with n-heptane (2.0 L), and dried in vacuum at below 50° C. to constant weight to afford anhydrous crystalline 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (586 g, 95%) as a white solid. ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

Example 8. 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile Monohydrate

A suspension of anhydrous crystalline 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (585 g, 1.71 mol) in water (5.9 L) was stirred at room temperature for 2 h. When XRPD confirmed that the conversion of the anhydrous crystalline form to the monohydrate crystalline form was complete, the solids were collected by filtration and washed with water (2.9 L). The wet cake was dried at 20-50° C. either in a vacuum oven or by pulling a vacuum from the filter until the water content analyzed by KF was 5±0.3% to afford crystalline 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate (602 g, 98%) as a white solid. ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; LCMS Calculated for: C₁₇H₁₈N₄O₂S: 342.4, Found: 343 (M⁺+H); Water content: 5.15%.

Example 9. 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (Anhydrous Crystalline Free Base)

A solution of amorphous ((2R,5S)-5-{2-[(1R)-1-hydroxyethyl]-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl}tetrahydro-2H-pyran-2-yl)acetonitrile (84.5 g, 247 mmol) in methanol (MeOH, 800 mL) was polish filtered and transferred into a 5-neck 5 L round bottom flask equipped with a reflux condenser. Additional 200 mL of methanol was used to wash the filter funnel. To the resulted methanol solution, ethyl acetate (2000 mL) was added and the resulting clear solution was heated to 70° C. over 30 minutes. The mixture of methanol and ethyl acetate was then distilled at atmospheric pressure. An additional 2000 mL of ethyl acetate was added when the collected solvent mixture reached 1700 mL and the atmospheric distillation was continued. When the total collected solvent mixture reached 4000 mL (in about 8 h), the remaining solution in the flask became cloudy and solids gradually formed. The atmospheric distillation was continued until the total collected solvent mixture reached 4250 mL, and the remaining solvent mixture, mainly ethyl acetate, in the flask was about 750 mL. n-Heptane (1150 mL) was then added slowly to the flask at approximately 70° C. (EtOAc to n-Heptane approximately at 1 to 1.5), and the resulting mixture was gradually cooled to room temperature. The mixture was agitated at room temperature for an additional 2-3 h to initiate crystallization. The solids were collected by filtration, washed with n-heptane (2×300 mL), and dried at 50° C. in vacuum oven with N₂ sweeping to afford ((2R,5S)-5-{2-[(1R)-1-hydroxyethyl]-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl}tetrahydro-2H-pyran-2-yl)acetonitrile (78.1 g, 92.4%) as white anhydrous crystalline powder.

C₁₇H₁₈N₄O₂S (MW 342.42), LCMS (EI) m/e 343 (M⁺+H); ¹H NMR (400 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.97 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.30 (t, J=11.0 Hz, 1H), 4.17 (s, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.86 (dd, J=17.0, 6.6 Hz, 1H), 2.76-2.56 (m, 1H), 2.19 (d, J=10.6 Hz, 1H), 2.06 (d, J=13.2 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (100 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm.; water content by KF: 1.15% by weight. The DSC thermogram shown in FIG. 1 revealed one endothermic event with an onset at 185.05° C., which relates to the compound melting, and the peak at 189.71° C. The endothermic event at about 260° C. associated with the decomposition of the compound. The TGA thermogram shown in FIG. 2 revealed a weight loss of 1.25% up to 200° C. Significant weight loss was observed at temperatures above 200° C. due to decomposition of the compound. The XRPD pattern was determined for the title compound and is shown in FIG. 3. A list of 2-theta peaks is provided in Table 2 below.

TABLE 2 Net Gross Relative 2-Theta d (A) Intensity Intensity Intensity (%) 6.608 13.3654 608 931 2.7 8.802 10.0379 8330 8970 37.6 9.699 9.1114 1560 2280 7.0 10.016 8.8244 2260 3010 10.2 10.574 8.3595 6020 6800 27.2 13.207 6.6983 2970 3870 13.4 14.509 6.1000 1490 2560 6.7 15.092 5.8659 3980 5180 18.0 16.329 5.4241 21900 23300 98.8 16.889 5.2454 1350 2870 6.1 17.554 5.0482 5510 7120 24.9 18.017 4.9194 4010 5680 18.1 19.081 4.6474 11000 12800 49.6 19.726 4.4971 3490 5320 15.8 21.174 4.1927 7880 9770 35.6 21.648 4.1018 2740 4640 12.4 22.466 3.9544 1080 2980 4.9 23.387 3.8007 3290 5160 14.9 24.037 3.6993 12100 13900 54.7 25.096 3.5456 626 2370 2.8 26.204 3.3980 5000 6720 22.6 26.420 3.3708 6510 8220 29.4 26.858 3.3169 1190 2880 5.4 27.681 3.2201 1320 2970 6.0 27.933 3.1916 1200 2830 5.4 29.318 3.0439 1060 2600 4.8 31.169 2.8672 1510 2870 6.8 31.300 2.8555 1560 2910 7.1 33.466 2.6755 607 1730 2.7 35.550 2.5233 826 1820 3.7 40.831 2.2083 501 1450 2.3 41.961 2.1514 966 1920 4.4 44.759 2.0232 618 1520 2.8 51.694 1.7669 229 1020 1.0

Example 10. 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile Monohydrate

In a 2-L round bottom flask equipped with a reflux condenser, a thermocouple and a magnetic stirring bar, was charged amorphous 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile (93.0 g, 272 mmol) and isopropyl alcohol (IPA, 1116 mL) at room temperature. The resulting suspension was heated to 50-55° C. to obtain a clear solution. The solution was polish filtered through a filter funnel at 50° C. An additional amount of isopropyl alcohol (IPA, 47 mL) was used to wash the filter funnel. To the combined solution was added water (930 mL) over 30 minutes while maintaining the internal temperature at 45-50° C. White precipitate gradually appeared upon the addition of the water. The IPA was removed by rotary evaporation under vacuum with a water bath at 50° C. During the distillation, an additional amount of water (1209 mL) was added to keep the total volume of the mixture at about 1500 mL. After the vacuum distillation, the resulting mixture was gradually cooled to room temperature and agitated at room temperature for 1-2 h. The solids were collected by filtration, washed with water (186 mL), and dried on a filter funnel with a housing vacuum at room temperature for 16 h to afford 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile monohydrate (91.6 g, 94%) as white crystalline powder. ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.42), LCMS (D) m/e 343 (M⁺+H). Water content by KF: 5.15% by weight. The melting/decomposition range was determined by DSC and is shown in FIG. 4. The DSC thermogram revealed one dehydration endothermic event with an onset at 69.37° C. and the peak at 106.41° C., followed by the melting with an onset at 131.01° C. and a peak at 139.99° C. The TGA thermogram (FIG. 5) showed a weight loss of 4.9% up to 150° C., which corresponds to the water content of the mono-hydrate. After 200° C. the compound starts to decompose. The XRPD pattern was determined for the title compound and is shown in FIG. 6. A list of 2-theta peaks is provided in Table 3 below.

TABLE 3 Net Gross Relative 2-Theta d (A) Intensity Intensity Intensity (%) 8.477 10.4224 28200 28700 91.9 8.678 10.1819 14500 15000 47.3 11.368 7.7776 2600 3320 8.5 13.150 6.7274 564 1320 1.8 13.568 6.5211 162 922 0.5 14.592 6.0656 23400 24300 76.1 15.064 5.8765 21200 22100 69.0 15.789 5.6082 9180 10100 29.9 16.917 5.2369 6130 7140 19.9 17.427 5.0846 3000 4020 9.8 18.599 4.7668 7670 8720 25.0 19.388 4.5747 20300 21400 66.2 20.160 4.4011 4640 5700 15.1 21.091 4.2089 6690 7710 21.8 21.463 4.1368 839 1840 2.7 22.460 3.9554 3070 4150 10.0 22.871 3.8853 1370 2510 4.5 23.366 3.8040 6710 7900 21.8 23.503 3.7822 8550 9750 27.8 24.518 3.6279 706 2000 2.3 25.065 3.5499 29900 31200 97.3 25.674 3.4670 3830 5200 12.4 25.878 3.4401 11100 12500 36.2 26.306 3.3857 12500 13900 40.7 26.547 3.3549 18100 19500 58.9 27.574 3.2323 6810 8210 22.2 28.299 3.1511 717 2100 2.3 28.625 3.1160 3130 4490 10.2 29.200 3.0559 1670 3000 5.4 29.828 2.9930 1100 2370 3.6 30.451 2.9332 3810 5010 12.4 30.715 2.9085 5430 6600 17.7 31.001 2.8823 1830 2960 6.0 31.335 2.8524 1820 2910 5.9 32.496 2.7531 420 1420 1.4 33.388 2.6815 4050 5030 13.2 34.026 2.6327 1220 2180 4.0 34.291 2.6130 861 1800 2.8 35.285 2.5416 724 1630 2.4 35.729 2.5111 1990 2900 6.5 36.639 2.4507 684 1590 2.2 36.931 2.4320 744 1640 2.4 37.470 2.3983 2760 3630 9.0 37.686 2.3850 1160 2020 3.8 39.059 2.3043 567 1430 1.8 39.713 2.2678 767 1680 2.5 40.791 2.2103 908 1870 3.0 41.862 2.1563 2100 3070 6.8 42.406 2.1298 511 1470 1.7 43.684 2.0704 531 1430 1.7 44.647 2.0280 1760 2680 5.7 45.207 2.0042 462 1430 1.5 45.857 1.9773 428 1430 1.4 47.419 1.9157 1510 2540 4.9 47.976 1.8947 1750 2780 5.7 48.744 1.8667 896 1890 2.9 49.480 1.8406 470 1420 1.5 51.479 1.7737 811 1630 2.6 52.307 1.7476 452 1270 1.5 53.685 1.7060 321 1130 1.0

Example 11. Dynamic Vapor Sorption

A Dynamic Vapor Sorption (DVS) study was conducted on the compound of Example 9 to monitor the hydroscopicity, hydrate formation and dehydration, as well as solid form transformation. The moisture uptake profile was completed in four cycles in 10% relative humidity (RH) increments with the first adsorption from 25% to 95% RH, followed by desorption in 10% increments from 95% to 5% RH. The equilibration criteria were as follows: 0.0050 wt % in 5 minutes with a maximum equilibration time of 180 minutes. All adsorption and desorption were performed at room temperature (25° C.). No pre-drying step was applied for the sample. Water absorption of the anhydrous form was slow below 85% RH and fast above 85% RH. Changes in the XRPD patterns before and after DVS suggest solid form change. After DVS cycle 4, the anhydrous form was fully converted to the hydrate form. Under ambient storage conditions, the anhydrous form will slowly absorb water and convert to hydrate form. The dehydration process from the hydrate to the anhydrous form is very slow, even at 5% RH. The hydrate form is physically stable in a wide range of humidity conditions. Vapor sorption/desorption isotherms are shown in FIG. 7 and FIG. 8. An XRPD pattern overlay before and after DVS is shown in FIG. 9.

Example 12. Humidity Chamber Study A

The compound of Example 9 was placed in a humidity chamber set at 40° C. and 75% relative humidity for 5 days. The resulting sample was analyzed by XRPD, TGA, and DSC as shown in FIGS. 10 to 12. Based on XRPD data, the anhydrous crystalline free base was converted to the crystalline hydrate form. The water content by KF was 4.6% and the weight loss observed by TGA was 5.01%.

Example 13. Humidity Chamber Study B

The compound of Example 9 was placed in a humidity chamber set at 30° C. and 90% relative humidity (RH) for 7 days. The resulting sample was analyzed by XRPD, TGA, and DSC as shown in FIGS. 13 to 15. Based on XRPD, the anhydrous crystalline free base was converted to the crystalline hydrate form. The XRPD patterns of the 30° C./90% RH sample corresponded to the hydrate form obtained from an aqueous suspension of the anhydrous crystalline free base drug substance. The water content by KF was 4.72% and the weight loss observed by TGA was 5.05%.

Example 14. (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole

Step 1. (R)-2,2,5-Trimethyloxazolidin-4-one

To a solution of (2R)-2-hydroxypropanamide (30 g, 337 mmol) in acetone was added 2,2-dimethoxypropane (51.8 mL, 421 mmol, 1.25 equiv) and boron trifluoride diethyl etherate (BF₃-Et₂O, 92.13 mL, 16.8 mmol, 0.05 equiv) at room temperature. The resulting reaction mixture was then stirred at room temperature overnight. When TLC indicated the reaction was complete, the solvent was removed under reduced pressure at below 35° C. and the residue was added to methyl t-butyl ether (MTBE, 350 mL). The solution was treated with saturated aqueous sodium bicarbonate (NaHCO₃) solution (15 mL), solid sodium bicarbonate (NaHCO₃, 4 g), and solid sodium sulfate (Na₂SO₄, 30 g) and the resulting mixture was stirred at room temperature for 30 minutes. The solids were filtered off and washed with methyl t-butyl ether (MTBE, 50 mL). The two phases of the combined filtrates were separated and the organic phase was washed with water (30 mL) and dried with sodium sulfate (Na₂SO₄, 20 g). After removal of the drying agent, the filtrate was concentrated under reduced pressure and the solvent was switched into n-hexane to provide desired product. The solids were collected by filtration, washed with n-hexane and dried to give the desired product, (R)-2,2,5-trimethyloxazolidin-4-one, (42 g, 97%) as white crystalline solids. ¹H NMR (400 MHz, CD₂Cl₂) δ 7.66 (s, 1H), 4.37 (q, J=6.7 Hz, 1H), 1.47 (s, 3H), 1.44 (s, 3H), 1.36 (d, J=6.7 Hz, 3H) ppm; ¹³C NMR (101 MHz, CD₂Cl₂) δ 175.58 (s), 90.70 (s), 73.76 (s), 29.97 (s), 28.52 (s), 18.60 (s) ppm.

Step 2. (R)-4-Methoxy-2,2,5-trimethyl-2,5-dihydrooxazole

To a solution of (R)-2,2,5-trimethyloxazolidin-4-one (20 g, 155 mmol) in dichloromethane (DCM, 200 mL) was added trimethoxonium tetrafluoride (Me₃O⁺BF₄ ⁻, 24.1 g, 155 mmol, 1.0 equiv) at room temperature. The resulting reaction mixture was stirred at room temperature for 6 hours. When ¹H-NMR indicated the reaction was complete, the reaction mixture was added to dichloromethane (DCM, 100 mL) and cooled to 0-5° C. The resulting solution was then treated with a 2M aqueous sodium carbonate solution (Na₂CO₃, 230 mL) while maintaining the internal temperature at 0-5° C. The two phases were separated and the organic phase was washed with water (2×100 mL), dried over sodium sulfate (Na₂SO₄, 50 g), and concentrated under reduced pressure to give the crude desired product, (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole, (19 g, 87%) as yellow oil, which can be directly used for the subsequent reaction without further purification. The pure desired product (12 g; bp 50° C. at 50 mba) was obtained by vacuum distillation as colorless oil. ¹H NMR (400 MHz, CD₂Cl₂) δ 4.58 (q, J=6.6 Hz, 1H), 3.80 (s, 3H), 1.41 (s, 3H), 1.35 (s, 3H), 1.29 (d, J=6.6 Hz, 3H) ppm; ¹³C NMR (101 MHz, CD₂Cl₂) δ 169.80 (s), 103.90 (s), 75.08 (s), 56.46 (s), 30.50 (s), 28.69 (s), 20.07 (s) ppm.

Example 15. Alternative preparation of 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile

To a flask was added (R)-2,2,5-trimethyloxazolidin-4-one (6.7 g, 52 mmol), trimethyloxonium tetrafluoroborate (Me₃O⁺BF₄ ⁻, 7.7 g, 52 mmol), and anhydrous dichloromethane (DCM, 50 mL) at room temperature. The resulting mixture was stirred at room temperature for 2 hours. When ¹H NMR revealed that the formation of (R)-4-methoxy-2,2,5-trimethyl-2,5-dihydrooxazole was complete, the reaction mixture was charged with a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (Example 4, 5.0 g, 17.3 mmol) at room temperature. The solvent was then switched into methanol (80 mL) by addition of methanol to the reaction mixture and distillation to remove dichloromethane. The resulting reaction mixture was then heated to 65° C. for 1.5 hours. When HPLC showed the reaction was complete, the solvent was removed under reduced pressure and the residue was treated with dichloromethane (80 mL). The resulting mixture was then treated with saturated aqueous sodium bicarbonate solution (NaHCO₃, 10 mL) followed by solid NaHCO₃ (11.6 g, 139 mmol) before being stirred at room temperature for 30 min. The mixture was dried over Na₂SO₄ and the liquid was filtered. The solids were removed by filtration and the two phases of the filtrate were separated. The organic phase was washed with water (2×25 mL), dried over Na₂SO₄, and concentrated. The residue was then dissolved in 0.1 M aqueous hydrochloric acid (HCl) and the resulting acidic aqueous solution was washed with dichloromethane (2×20 mL). The acidic aqueous solution was then neutralized with NaHCO₃ to precipitate the crude desired product. The solids were collected by filtration, washed with water, and dried to give the desired product (5.0 g, 84% yield) as a mixture of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile.

The mixture of two diastereomers is inseparable by silica gel column chromatography and was used directly in the subsequent reaction (see, e.g., Example 6) without further separation.

For (2R,5S)-isomer: ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

For (2S,5S)-isomer: ¹H NMR (400 MHz, CD₃CN) δ 8.93 (s, 1H), 7.80 (d, J=5.5 Hz, 1H), 7.63 (d, J=5.5 Hz, 1H), 5.38 (s, 1H), 5.00 (dq, J=9.4, 4.7 Hz, 1H), 4.43 (dd, J=11.8, 9.3 Hz, 1H), 4.26 (dd, J=8.6, 3.7 Hz, 1H), 4.16 (s, 1H), 4.03-3.89 (m, 1H), 3.17 (dd, J=17.1, 8.6 Hz, 1H), 2.87 (dd, J=17.2, 5.4 Hz, 1H), 2.57 (dtd, J=14.8, 10.8, 4.2 Hz, 1H), 2.20-1.99 (m, 2H), 1.88-1.82 (m, 1H), 1.73 (d, J=6.4 Hz, 3H) ppm; ¹³C NMR (101 MHz, CD₃CN) δ 158.04, 152.88, 142.12, 136.81, 136.46, 127.44, 127.14, 119.04, 116.97, 70.00, 64.83, 64.03, 54.55, 28.06, 25.73, 22.46, 21.94 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

Example 16. Alternative preparation of 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile

Step 1. (R)-1-Amino-1-oxopropan-2-yl Acetate

To a 1-L 3-necked round bottom flask equipped with a reflux condenser, a nitrogen inlet, a thermal couple and a magnetic stirring bar under nitrogen was charged (R)-2-hydroxypropanamide (49.95 g, 543.8 mmol) and tetrahydrofuran 300 mL) at room temperature. The resulting yellow solution was cooled to 0-5° C. by an ice-water bath before acetyl chloride (40.60 mL, 571.0 mmol, 1.05 equiv) was charged while maintaining the internal temperature at below 20° C. After the internal temperature was dropped back to below 5° C., 4-methylmorpholine (59.2 mL, 538.0 mmol, 0.99 equiv) was charged while maintaining the internal temperature to below 10° C. The resulting reaction mixture was then stirred at room temperature for 4 hours before the mixture was filtered to remove the solids. The solids were washed with THF (60 mL) and the filtrate was concentrated under reduced pressure to provide the crude desired product, (R)-1-amino-1-oxopropan-2-yl acetate, (75.0 g, 105.2%) as a white to off-white solid, which was used directly in next reaction without further purification. ¹H NMR (400 MHz, DMSO-d₆) δ 7.42 (s, 1H), 7.14 (s, 1H), 4.84 (q, J=7.6 Hz, 1H), 2.03 (s, 3H), 1.29 (d, J=7.6 Hz, 3H) ppm.

Step 2. (R)-1-Cyanoethyl Acetate

To a 3-L 3-necked round bottom flask equipped with a reflux condenser, a nitrogen inlet, a thermal couple and a magnetic stirring bar under nitrogen was charged crude (R)-1-amino-1-oxopropan-2-yl acetate (70.0 g, 533.8 mmol) and N,N-dimethylformamide (DMF, 280 mL) at room temperature. The resulting light yellow solution was then treated with cyanuric chloride (44.0 g, 240.0 mmol) in 2-methoxy-2-methylpropane (TBME, 600 mL) at room temperature. The reaction mixture was stirred at room temperature for 16 hours. The white solids were filtered and washed with TBME (800 mL). The combined organic filtrates were washed sequentially with saturated aqueous sodium bicarbonate solution (NaHCO₃, 200 mL), water (4×200 mL), and brine (100 mL). The resultant organic phase was then dried with anhydrous MgSO₄ (15 g) and concentrated under reduced pressure to provide the crude desired product, (R)-1-cyanoethyl acetate, (42.03 g, 69.6%) as a colorless to light yellow oil, which was used directly in the subsequent reaction without further purification. NMR (400 MHz, DMSO-d₆) δ 5.46 (q, J=7.6 Hz, 1H), 2.09 (s, 3H), 1.53 (d, J=7.6 Hz, 3H) ppm.

Step 3. (R)-ethyl 2-hydroxypropanimidate

To a 100-mL round bottom flask equipped with a magnetic stirring bar was charged crude (R)-1-cyanoethyl acetate (1.021 g, 8.665 mmol) and ethanol (EtOH, 1.518 mL, 26.0 mmol) at room temperature. The resulting solution was then cooled to −40° C. before being bubbled in hydrogen chloride (HCl) gas for 45 seconds. The reaction mixture was then gradually warmed to room temperature. After 16 hours, the reaction mixture was cooled to 0° C. before tetrahydrofuran (THF, 2.0 mL, 25 mmol) and 4-methylmorpholine (0.865 mL, 7.87 mmol) were sequentially charged. The solids were removed by filtration and the crude desired product, (R)-ethyl 2-hydroxypropanimidate, in the filtrate was used directly in the subsequent reaction without further purification. ¹H NMR (300 MHz, DMSO-d₆) δ 11.14 (s, 1H), 4.52-4.40 (m, 3H), 1.36-1.31 (m, 6H) ppm.

Step 4. 2-((2R,5S)-5-(2-((R)-1-Hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile

To a 3-necked 100-mL round bottom flask equipped with a nitrogen inlet, a thermocouple and a magnetic stirring bar under nitrogen was charged a mixture of 2-((2R,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(6-aminothieno[3,2-b]pyridin-7-ylamino)tetrahydro-2H-pyran-2-yl)acetonitrile (Example 4, 0.30 g, 1.04 mmol) in ethanol (EtOH, 4.0 mL) at room temperature. The mixture was then heated to 80° C. to provide a clear solution before a solution of the crude (R)-ethyl 2-hydroxypropanimidate in THF generated in previous step was added to the ethanol solution at 80° C. When the reaction was completed after 1 hour as indicated by HPLC, the reaction mixture was cooled to room temperature. The cooled reaction mixture was filtered and the filtrate was concentrated under reduced pressure to afford the crude desired product (0.3 g, 84% yield) as a mixture of 2-((2R,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile and 2-((2S,5S)-5-(2-((R)-1-hydroxyethyl)-1H-imidazo[4,5-d]thieno[3,2-b]pyridin-1-yl)tetrahydro-2H-pyran-2-yl)acetonitrile, which is inseparable by silica gel column chromatography and was used directly in the subsequent reaction without further separation (see, e.g., Example 6).

For (2R,5S)-isomer: ¹H NMR (500 MHz, DMSO-d₆) δ 9.00 (s, 1H), 8.03 (d, J=5.5 Hz, 1H), 7.69 (d, J=5.5 Hz, 1H), 5.96 (s, 1H), 5.22 (s, 1H), 5.11 (s, 1H), 4.31 (t, J=11.0 Hz, 1H), 4.22-4.08 (m, 1H), 4.02 (s, 1H), 2.96 (dd, J=17.0, 4.2 Hz, 1H), 2.84 (dd, J=17.0, 6.6 Hz, 1H), 2.65 (qd, J=12.7, 4.3 Hz, 1H), 2.19 (d, J=10.0 Hz, 1H), 2.06 (d, J=13.4 Hz, 1H), 1.72 (dd, J=12.6, 3.7 Hz, 1H), 1.66 (d, J=6.5 Hz, 3H) ppm; ¹³C NMR (101 MHz, DMSO-d₆) δ 157.95, 152.11, 141.57, 136.18, 135.24, 127.98, 126.79, 119.08, 116.12, 72.42, 68.87, 62.95, 51.67, 30.39, 28.44, 24.09, 22.36 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

For (2S,5S)-isomer: ¹H NMR (400 MHz, CD₃CN) δ 8.93 (s, 1H), 7.80 (d, J=5.5 Hz, 1H), 7.63 (d, J=5.5 Hz, 1H), 5.38 (s, 1H), 5.00 (dq, J=9.4, 4.7 Hz, 1H), 4.43 (dd, J=11.8, 9.3 Hz, 1H), 4.26 (dd, J=8.6, 3.7 Hz, 1H), 4.16 (s, 1H), 4.03-3.89 (m, 1H), 3.17 (dd, J=17.1, 8.6 Hz, 1H), 2.87 (dd, J=17.2, 5.4 Hz, 1H), 2.57 (dtd, J=14.8, 10.8, 4.2 Hz, 1H), 2.20-1.99 (m, 2H), 1.88-1.82 (m, 1H), 1.73 (d, J=6.4 Hz, 3H) ppm; ¹³C NMR (101 MHz, CD₃CN) δ 158.04, 152.88, 142.12, 136.81, 136.46, 127.44, 127.14, 119.04, 116.97, 70.00, 64.83, 64.03, 54.55, 28.06, 25.73, 22.46, 21.94 ppm; C₁₇H₁₈N₄O₂S (MW 342.4), LCMS (EI) m/e 343 (M⁺+H).

Example A: In Vitro JAK Kinase Assay

Compounds herein were tested for inhibitory activity of JAK targets according to the following in vitro assay described in Park et al., Analytical Biochemistry 1999, 269, 94-104. The catalytic domains of human JAK1 (a. a. 837-1142), JAK2 (a. a. 828-1132) and JAK3 (a. a. 781-1124) were expressed using baculovirus in insect cells and purified. The catalytic activity of JAK1, JAK2 or JAK3 was assayed by measuring the phosphorylation of a biotinylated peptide. The phosphorylated peptide was detected by homogenous time resolved fluorescence (HTRF). IC₅₀s of compounds were measured for each kinase in the 40 μL, reactions that contain the enzyme, ATP and 500 nM peptide in 50 mM Tris (pH 7.8) buffer with 100 mM NaCl, 5 mM DTT, and 0.1 mg/mL (0.01%) BSA. For the 1 mM IC₅₀ measurements, ATP concentration in the reactions was 1 mM. Reactions were carried out at room temperature for 1 hour and then stopped with 20 μL 45 mM EDTA, 300 nM SA-APC, 6 nM Eu-Py20 in assay buffer (Perkin Elmer, Boston, Mass.). Binding to the Europium labeled antibody took place for 40 minutes and HTRF signal was measured on a PHERA star plate reader (BMG, Cary, N.C.). The compound of Formula Ia was tested in the Example A assay at 1 mM ATP and found to have an IC₅₀ at JAK1 of ≤100 nM and an IC₅₀ at JAK2 of ≤1000 nM with a JAK2/JAK1 ratio >10.

Example B: Cellular Assays

Cancer cell lines dependent on cytokines and hence JAK/STAT signal transduction, for growth, can be plated at 6000 cells per well (96 well plate format) in RPMI 1640, 10% FBS, and 1 nG/mL of appropriate cytokine. Compounds can be added to the cells in DMSO/media (final concentration 0.2% DMSO) and incubated for 72 hours at 37° C., 5% CO₂. The effect of compound on cell viability is assessed using the CellTiter-Glo Luminescent Cell Viability Assay (Promega) followed by TopCount (Perkin Elmer, Boston, Mass.) quantitation. Potential off-target effects of compounds are measured in parallel using a non-JAK driven cell line with the same assay readout. All experiments are typically performed in duplicate.

The above cell lines can also be used to examine the effects of compounds on phosphorylation of JAK kinases or potential downstream substrates such as STAT proteins, Akt, Shp2, or Erk. These experiments can be performed following an overnight cytokine starvation, followed by a brief preincubation with compound (2 hours or less) and cytokine stimulation of approximately 1 hour or less. Proteins are then extracted from cells and analyzed by techniques familiar to those schooled in the art including Western blotting or ELISAs using antibodies that can differentiate between phosphorylated and total protein. These experiments can utilize normal or cancer cells to investigate the activity of compounds on tumor cell survival biology or on mediators of inflammatory disease. For example, with regards to the latter, cytokines such as IL-6, IL-12, IL-23, or IFN can be used to stimulate JAK activation resulting in phosphorylation of STAT protein(s) and potentially in transcriptional profiles (assessed by array or qPCR technology) or production and/or secretion of proteins, such as IL-17. The ability of compounds to inhibit these cytokine mediated effects can be measured using techniques common to those schooled in the art. To assess compound effects on JAK2, primary cells or cell lines can be stimulated with JAK2-dependent growth factors such as GM-CSF or Tpo, proteins extracted from cells and analyzed by techniques familiar to those schooled in the art including Western blotting or ELISAs using antibodies that can differentiate between phosphorylated and total protein.

Compounds herein can also be tested in cellular models designed to evaluate their potency and activity against mutant JAKs, for example, the JAK2V617F mutation found in myeloid proliferative disorders. These experiments often utilize cytokine dependent cells of hematological lineage (e.g. BaF/3) into which the wild-type or mutant JAK kinases are ectopically expressed (James, C., et al. Nature 434:1144-1148; Staerk, J., et al. JBC 280:41893-41899). Endpoints include the effects of compounds on cell survival, proliferation, and phosphorylated JAK, STAT, Akt, or Erk proteins.

Certain compounds herein can be evaluated for their activity inhibiting T-cell proliferation. Such as assay can be considered a second cytokine (i.e. JAK) driven proliferation assay and also a simplistic assay of immune suppression or inhibition of immune activation. The following is a brief outline of how such experiments can be performed. Peripheral blood mononuclear cells (PBMCs) are prepared from human whole blood samples using Ficoll Hypaque separation method and T-cells (fraction 2000) can be obtained from PBMCs by elutriation. Freshly isolated human T-cells can be maintained in culture medium (RPMI 1640 supplemented with 10% fetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin) at a density of 2×10⁶ cells/ml at 37° C. for up to 2 days. For IL-2 stimulated cell proliferation analysis, T-cells are first treated with Phytohemagglutinin (PHA) at a final concentration of 10 μg/mL for 72 hours. After washing once with PBS, 6000 cells/well are plated in 96-well plates and treated with compounds at different concentrations in the culture medium in the presence of 100 U/mL human IL-2 (ProSpec-Tany TechnoGene; Rehovot, Israel). The plates are incubated at 37° C. for 72 h and the proliferation index is assessed using CellTiter-Glo Luminescent reagents following the manufactory suggested protocol (Promega; Madison, Wis.).

Example C: In Vivo Anti-Tumor Efficacy

Compounds herein can be evaluated in human tumor xenograft models in immune compromised mice. For example, a tumorigenic variant of the INA-6 plasmacytoma cell line can be used to inoculate SCID mice subcutaneously (Burger, R., et al. Hematol J. 2:42-53, 2001). Tumor bearing animals can then be randomized into drug or vehicle treatment groups and different doses of compounds can be administered by any number of the usual routes including oral, i.p., or continuous infusion using implantable pumps. Tumor growth is followed over time using calipers. Further, tumor samples can be harvested at any time after the initiation of treatment for analysis as described above (Example B) to evaluate compound effects on JAK activity and downstream signaling pathways. In addition, selectivity of the compound(s) can be assessed using xenograft tumor models that are driven by other know kinases (e.g. Bcr-Abl) such as the K562 tumor model.

Example D: Murine Skin Contact Delayed Hypersensitivity Response Test

Compounds herein can also be tested for their efficacies (of inhibiting JAK targets) in the T-cell driven murine delayed hypersensitivity test model. The murine skin contact delayed-type hypersensitivity (DTH) response is considered to be a valid model of clinical contact dermatitis, and other T-lymphocyte mediated immune disorders of the skin, such as psoriasis (Immunol Today. 1998 January; 19(1):37-44). Murine DTH shares multiple characteristics with psoriasis, including the immune infiltrate, the accompanying increase in inflammatory cytokines, and keratinocyte hyperproliferation. Furthermore, many classes of agents that are efficacious in treating psoriasis in the clinic are also effective inhibitors of the DTH response in mice (Agents Actions. 1993 January; 38(1-2):116-21).

On Day 0 and 1, Balb/c mice are sensitized with a topical application, to their shaved abdomen with the antigen 2,4,dinitro-fluorobenzene (DNFB). On day 5, ears are measured for thickness using an engineer's micrometer. This measurement is recorded and used as a baseline. Both of the animals' ears are then challenged by a topical application of DNFB in a total of 20 μL (10 μL on the internal pinna and 10 μL on the external pinna) at a concentration of 0.2%. Twenty-four to seventy-two hours after the challenge, ears are measured again. Treatment with the test compounds is given throughout the sensitization and challenge phases (day −1 to day 7) or prior to and throughout the challenge phase (usually afternoon of day 4 to day 7). Treatment of the test compounds (in different concentration) is administered either systemically or topically (topical application of the treatment to the ears). Efficacies of the test compounds are indicated by a reduction in ear swelling comparing to the situation without the treatment. Compounds causing a reduction of 20% or more were considered efficacious. In some experiments, the mice are challenged but not sensitized (negative control).

The inhibitive effect (inhibiting activation of the JAK-STAT pathways) of the test compounds can be confirmed by immunohistochemical analysis. Activation of the JAK-STAT pathway(s) results in the formation and translocation of functional transcription factors. Further, the influx of immune cells and the increased proliferation of keratinocytes should also provide unique expression profile changes in the ear that can be investigated and quantified. Formalin fixed and paraffin embedded ear sections (harvested after the challenge phase in the DTH model) are subjected to immunohistochemical analysis using an antibody that specifically interacts with phosphorylated STAT3 (clone 58E12, Cell Signaling Technologies). The mouse ears are treated with test compounds, vehicle, or dexamethasone (a clinically efficacious treatment for psoriasis), or without any treatment, in the DTH model for comparisons. Test compounds and the dexamethasone can produce similar transcriptional changes both qualitatively and quantitatively, and both the test compounds and dexamethasone can reduce the number of infiltrating cells. Both systemically and topical administration of the test compounds can produce inhibitive effects, i.e., reduction in the number of infiltrating cells and inhibition of the transcriptional changes.

Example E: In Vivo Anti-Inflammatory Activity

Compounds herein can be evaluated in rodent or non-rodent models designed to replicate a single or complex inflammation response. For instance, rodent models of arthritis can be used to evaluate the therapeutic potential of compounds dosed preventatively or therapeutically. These models include but are not limited to mouse or rat collagen-induced arthritis, rat adjuvant-induced arthritis, and collagen antibody-induced arthritis. Autoimmune diseases including, but not limited to, multiple sclerosis, type I-diabetes mellitus, uveoretinitis, thyroiditis, myasthenia gravis, immunoglobulin nephropathies, myocarditis, airway sensitization (asthma), lupus, or colitis may also be used to evaluate the therapeutic potential of compounds herein. These models are well established in the research community and are familiar to those schooled in the art (Current Protocols in Immunology, Vol 3, Coligan, J. E. et al, Wiley Press.; Methods in Molecular Biology: Vol. 225, Inflammation Protocols, Winyard, P. G. and Willoughby, D. A., Humana Press, 2003).

Example F: Animal Models for the Treatment of Dry Eye, Uveitis, and Conjunctivitis

Agents may be evaluated in one or more preclinical models of dry eye known to those schooled in the art including, but not limited to, the rabbit concanavalin A (ConA) lacrimal gland model, the scopolamine mouse model (subcutaneous or transdermal), the Botulinumn mouse lacrimal gland model, or any of a number of spontaneous rodent auto-immune models that result in ocular gland dysfunction (e.g. NOD-SCID, MRL/lpr, or NZB/NZW) (Barabino et al., Experimental Eye Research 2004, 79, 613-621 and Schrader et al., Developmental Opthalmology, Karger 2008, 41, 298-312, each of which is incorporated herein by reference in its entirety). Endpoints in these models may include histopathology of the ocular glands and eye (cornea, etc.) and possibly the classic Schirmer test or modified versions thereof (Barabino et al.) which measure tear production. Activity may be assessed by dosing via multiple routes of administration (e.g. systemic or topical) which may begin prior to or after measurable disease exists.

Agents may be evaluated in one or more preclinical models of uveitis known to those schooled in the art. These include, but are not limited to, models of experimental autoimmune uveitis (EAU) and endotoxin induced uveitis (EIU). EAU experiments may be performed in the rabbit, rat, or mouse and may involve passive or activate immunization. For instance, any of a number or retinal antigens may be used to sensitize animals to a relevant immunogen after which animals may be challenged ocuarly with the same antigen. The EIU model is more acute and involves local or systemic administration of lipopolysaccharide at sublethal doses. Endpoints for both the EIU and EAU models may include fundoscopic exam, histopathology amongst others. These models are reviewed by Smith et al. (Immunology and Cell Biology 1998, 76, 497-512, which is incorporated herein by reference in its entirety). Activity is assessed by dosing via multiple routes of administration (e.g. systemic or topical) which may begin prior to or after measurable disease exists. Some models listed above may also develop scleritis/episcleritis, chorioditis, cyclitis, or iritis and are therefore useful in investigating the potential activity of compounds for the therapeutic treatment of these diseases.

Agents may also be evaluated in one or more preclinical models of conjunctivitis known those schooled in the art. These include, but are not limited to, rodent models utilizing guinea-pig, rat, or mouse. The guinea-pig models include those utilizing active or passive immunization and/or immune challenge protocols with antigens such as ovalbumin or ragweed (reviewed in Groneberg, D. A., et al., Allergy 2003, 58, 1101-1113, which is incorporated herein by reference in its entirety). Rat and mouse models are similar in general design to those in the guinea-pig (also reviewed by Groneberg). Activity may be assessed by dosing via multiple routes of administration (e.g. systemic or topical) which may begin prior to or after measurable disease exists. Endpoints for such studies may include, for example, histological, immunological, biochemical, or molecular analysis of ocular tissues such as the conjunctiva.

Example G: In Vivo Protection of Bone

Compounds may be evaluated in various preclinical models of osteopenia, osteoporosis, or bone resorption known to those schooled in the art. For example, ovariectomized rodents may be used to evaluate the ability of compounds to affect signs and markers of bone remodeling and/or density (W. S. S. Jee and W. Yao, J Musculoskel. Nueron. Interact., 2001, 1(3), 193-207, which is incorporated herein by reference in its entirety). Alternatively, bone density and architecture may be evaluated in control or compound treated rodents in models of therapy (e.g. glucocorticoid) induced osteopenia (Yao, et al. Arthritis and Rheumatism, 2008, 58(6), 3485-3497; and id. 58(11), 1674-1686, both of which are incorporated herein by reference in its entirety). In addition, the effects of compounds on bone resorption and density may be evaluable in the rodent models of arthritis discussed above (Example E). Endpoints for all these models may vary but often include histological and radiological assessments as well as immunohisotology and appropriate biochemical markers of bone remodeling.

Example H: S100A9 Transgenic Mouse Model

It was previously shown that S100A9 transgenic mice display bone marrow accumulation of MDSC accompanied by development of progressive multilineage cytopenias and cytological dysplasia similar to MDS. Further, early forced maturation of MDSC by either all-trans-retinoic acid treatment or active immunoreceptor tyrosine-based activation motif-bearing (ITAM-bearing) adapter protein (DAP12) interruption of CD33 signaling rescued the hematologic phenotype and mitigated the disease. This system can be useful to test the effects on JAK1 inhibition on MDS-like disease in a preclinical model. J. Clin. Invest., 123(11):4595-4611 (2013), Accordingly, a JAK1 selective inhibitor is dosed by oral gavage. The compound's ability to reduce the cytopenias and cytological dysplasia observed in the S100A9 transgenic mice is monitored.

Various modifications of the invention, in addition to those described herein, will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. U.S. Ser. No. 14/068,796, filed Oct. 31, 2013, is incorporated herein by reference in its entirety. Each reference, including all patent, patent applications, and publications, cited in the present application is incorporated herein by reference in its entirety. 

What is claimed is:
 1. An anhydrous crystalline form of a compound of Formula Ia:

having an X-ray powder diffraction pattern substantially as shown in FIG.
 3. 2. An anhydrous crystalline form of a compound of Formula Ia:

having an X-ray powder diffraction pattern comprising at least one peak, in terms of 2θ, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°.
 3. The anhydrous crystalline form of claim 2, having an X-ray powder diffraction pattern comprising at least two peaks, in terms of 2θ, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°.
 4. The anhydrous crystalline form of claim 2, having an X-ray powder diffraction pattern comprising at least three peaks, in terms of 2θ, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°.
 5. The anhydrous crystalline form of claim 2, having an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2θ, selected from about 8.8°, about 10.5°, about 16.3°, about 17.5°, about 19.1°, about 21.2°, about 24.0°, and about 26.4°.
 6. The anhydrous crystalline form of claim 2, having an X-ray powder diffraction pattern comprising at least four peaks, in terms of 2θ, selected from about 8.8°, about 16.3°, about 19.1°, about 24.0°, and about 26.4°.
 7. The anhydrous crystalline form of claim 2, having a differential scanning calorimetry thermogram (DSC) substantially as shown in FIG.
 1. 8. The anhydrous crystalline form of claim 2, having a differential scanning calorimetry thermogram (DSC) characterized by an endothermic peak at about 185° C.
 9. The anhydrous crystalline form of claim 2, having a differential scanning calorimetry thermogram (DSC) characterized by an endothermic peak at about 190° C.
 10. The anhydrous crystalline form of claim 2, having a thermogravimetric analysis thermogram (TGA) substantially as shown in FIG.
 2. 11. The anhydrous crystalline form of claim 2, having a thermogravimetric analysis thermogram (TGA) characterized by a weight loss of about 1.25% up to 200° C.
 12. A composition comprising the anhydrous crystalline form of claim
 2. 13. The composition of claim 12, wherein the composition comprises at least one pharmaceutically acceptable carrier. 